Canonical Allele Identifier: CA2555016758
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784990G>A , CM000666.2:g.71784990G>A GRCh38
NC_000004.11:g.72650707G>A , CM000666.1:g.72650707G>A GRCh37
NC_000004.10:g.72869571G>A NCBI36
NG_012837.2:g.25531C>T
NG_012837.3:g.25531C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-936C>T ENSP00000421725.1:n.22-936C>T
ENST00000506245.1:c.-37+930C>T ENSP00000426718.1:n.-37+930C>T
NM_001204306.1:c.-36-936C>T NP_001191235.1:n.-36-936C>T
NM_001204307.1:c.22-936C>T NP_001191236.1:n.22-936C>T