Canonical Allele Identifier: CA1467386058
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785040A= , CM000666.2:g.71785040A= GRCh38
NC_000004.11:g.72650757A= , CM000666.1:g.72650757A= GRCh37
NC_000004.10:g.72869621A= NCBI36
NG_012837.2:g.25481T=
NG_012837.3:g.25481T=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-986T= ENSP00000421725.1:n.22-986T=
ENST00000506245.1:c.-37+880T= ENSP00000426718.1:n.-37+880T=
NM_001204306.1:c.-36-986T= NP_001191235.1:n.-36-986T=
NM_001204307.1:c.22-986T= NP_001191236.1:n.22-986T=