Canonical Allele Identifier: CA99074805
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs561637922
gnomAD v3: 4-71784937-T-C
gnomAD v4: 4-71784937-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784937T>C , CM000666.2:g.71784937T>C GRCh38
NC_000004.11:g.72650654T>C , CM000666.1:g.72650654T>C GRCh37
NC_000004.10:g.72869518T>C NCBI36
NG_012837.2:g.25584A>G
NG_012837.3:g.25584A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-883A>G ENSP00000421725.1:n.22-883A>G
ENST00000506245.1:c.-36-883A>G ENSP00000426718.1:n.-36-883A>G
NM_001204306.1:c.-36-883A>G NP_001191235.1:n.-36-883A>G
NM_001204307.1:c.22-883A>G NP_001191236.1:n.22-883A>G