Canonical Allele Identifier: CA1467386062
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785047C= , CM000666.2:g.71785047C= GRCh38
NC_000004.11:g.72650764C= , CM000666.1:g.72650764C= GRCh37
NC_000004.10:g.72869628C= NCBI36
NG_012837.2:g.25474G=
NG_012837.3:g.25474G=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-993G= ENSP00000421725.1:n.22-993G=
ENST00000506245.1:c.-37+873G= ENSP00000426718.1:n.-37+873G=
NM_001204306.1:c.-36-993G= NP_001191235.1:n.-36-993G=
NM_001204307.1:c.22-993G= NP_001191236.1:n.22-993G=