Canonical Allele Identifier: CA1467386045
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784996G= , CM000666.2:g.71784996G= GRCh38
NC_000004.11:g.72650713G= , CM000666.1:g.72650713G= GRCh37
NC_000004.10:g.72869577G= NCBI36
NG_012837.2:g.25525C=
NG_012837.3:g.25525C=

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-942C= ENSP00000421725.1:n.22-942C=
ENST00000506245.1:c.-37+924C= ENSP00000426718.1:n.-37+924C=
NM_001204306.1:c.-36-942C= NP_001191235.1:n.-36-942C=
NM_001204307.1:c.22-942C= NP_001191236.1:n.22-942C=