Canonical Allele Identifier: CA1467385982
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784863C= , CM000666.2:g.71784863C= GRCh38
NC_000004.11:g.72650580C= , CM000666.1:g.72650580C= GRCh37
NC_000004.10:g.72869444C= NCBI36
NG_012837.2:g.25658G=
NG_012837.3:g.25658G=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-809G= ENSP00000421725.1:n.22-809G=
ENST00000506245.1:c.-36-809G= ENSP00000426718.1:n.-36-809G=
NM_001204306.1:c.-36-809G= NP_001191235.1:n.-36-809G=
NM_001204307.1:c.22-809G= NP_001191236.1:n.22-809G=