Canonical Allele Identifier: CA2762139357
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785037T>C , CM000666.2:g.71785037T>C GRCh38
NC_000004.11:g.72650754T>C , CM000666.1:g.72650754T>C GRCh37
NC_000004.10:g.72869618T>C NCBI36
NG_012837.2:g.25484A>G
NG_012837.3:g.25484A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-983A>G ENSP00000421725.1:n.22-983A>G
ENST00000506245.1:c.-37+883A>G ENSP00000426718.1:n.-37+883A>G
NM_001204306.1:c.-36-983A>G NP_001191235.1:n.-36-983A>G
NM_001204307.1:c.22-983A>G NP_001191236.1:n.22-983A>G