Canonical Allele Identifier: CA1467386031
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784963A= , CM000666.2:g.71784963A= GRCh38
NC_000004.11:g.72650680A= , CM000666.1:g.72650680A= GRCh37
NC_000004.10:g.72869544A= NCBI36
NG_012837.2:g.25558T=
NG_012837.3:g.25558T=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-909T= ENSP00000421725.1:n.22-909T=
ENST00000506245.1:c.-36-909T= ENSP00000426718.1:n.-36-909T=
NM_001204306.1:c.-36-909T= NP_001191235.1:n.-36-909T=
NM_001204307.1:c.22-909T= NP_001191236.1:n.22-909T=