Canonical Allele Identifier: CA1467385981
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784864dup , CM000666.2:g.71784864dup GRCh38
NC_000004.11:g.72650581dup , CM000666.1:g.72650581dup GRCh37
NC_000004.10:g.72869445dup NCBI36
NG_012837.2:g.25659dup
NG_012837.3:g.25659dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-808dup ENSP00000421725.1:n.22-808dup
ENST00000506245.1:c.-36-808dup ENSP00000426718.1:n.-36-808dup
NM_001204306.1:c.-36-808dup NP_001191235.1:n.-36-808dup
NM_001204307.1:c.22-808dup NP_001191236.1:n.22-808dup