Canonical Allele Identifier: CA1467386092
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785136T= , CM000666.2:g.71785136T= GRCh38
NC_000004.11:g.72650853T= , CM000666.1:g.72650853T= GRCh37
NC_000004.10:g.72869717T= NCBI36
NG_012837.2:g.25385A=
NG_012837.3:g.25385A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-1082A= ENSP00000421725.1:n.22-1082A=
ENST00000506245.1:c.-37+784A= ENSP00000426718.1:n.-37+784A=
NM_001204306.1:c.-36-1082A= NP_001191235.1:n.-36-1082A=
NM_001204307.1:c.22-1082A= NP_001191236.1:n.22-1082A=