Canonical Allele Identifier: CA649007712
Gene: GC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785146A>G , CM000666.2:g.71785146A>G GRCh38
NC_000004.11:g.72650863A>G , CM000666.1:g.72650863A>G GRCh37
NC_000004.10:g.72869727A>G NCBI36
NG_012837.2:g.25375T>C
NG_012837.3:g.25375T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-1092T>C ENSP00000421725.1:n.22-1092T>C
ENST00000506245.1:c.-37+774T>C ENSP00000426718.1:n.-37+774T>C
NM_001204306.1:c.-36-1092T>C NP_001191235.1:n.-36-1092T>C
NM_001204307.1:c.22-1092T>C NP_001191236.1:n.22-1092T>C