Variant #0000000608 (NC_000002.11:g.29754808A>G, NM_004304.4:c.1127T>C (ALK))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.29754808A>G
Reference -
DB-ID ALK_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Admin
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Admin
Date created 2024-09-09 09:04:51 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALK NM_004304.4 ?/? - c.1127T>C r.(?) p.(Leu376Pro)