Canonical Allele Identifier: CA1064002689
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1742797938
gnomAD v3: 4-71784957-T-A
gnomAD v4: 4-71784957-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784957T>A , CM000666.2:g.71784957T>A GRCh38
NC_000004.11:g.72650674T>A , CM000666.1:g.72650674T>A GRCh37
NC_000004.10:g.72869538T>A NCBI36
NG_012837.2:g.25564A>T
NG_012837.3:g.25564A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-903A>T ENSP00000421725.1:n.22-903A>T
ENST00000506245.1:c.-36-903A>T ENSP00000426718.1:n.-36-903A>T
NM_001204306.1:c.-36-903A>T NP_001191235.1:n.-36-903A>T
NM_001204307.1:c.22-903A>T NP_001191236.1:n.22-903A>T