Canonical Allele Identifier: CA1467385995
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784886T= , CM000666.2:g.71784886T= GRCh38
NC_000004.11:g.72650603T= , CM000666.1:g.72650603T= GRCh37
NC_000004.10:g.72869467T= NCBI36
NG_012837.2:g.25635A=
NG_012837.3:g.25635A=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-832A= ENSP00000421725.1:n.22-832A=
ENST00000506245.1:c.-36-832A= ENSP00000426718.1:n.-36-832A=
NM_001204306.1:c.-36-832A= NP_001191235.1:n.-36-832A=
NM_001204307.1:c.22-832A= NP_001191236.1:n.22-832A=