Canonical Allele Identifier: CA1467385990
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784873A= , CM000666.2:g.71784873A= GRCh38
NC_000004.11:g.72650590A= , CM000666.1:g.72650590A= GRCh37
NC_000004.10:g.72869454A= NCBI36
NG_012837.2:g.25648T=
NG_012837.3:g.25648T=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-819T= ENSP00000421725.1:n.22-819T=
ENST00000506245.1:c.-36-819T= ENSP00000426718.1:n.-36-819T=
NM_001204306.1:c.-36-819T= NP_001191235.1:n.-36-819T=
NM_001204307.1:c.22-819T= NP_001191236.1:n.22-819T=