Canonical Allele Identifier: CA1467373187
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71756753G= , CM000666.2:g.71756753G= GRCh38
NC_000004.11:g.72622470G= , CM000666.1:g.72622470G= GRCh37
NC_000004.10:g.72841334G= NCBI36
NG_012837.2:g.53768C=
NG_012837.3:g.53768C=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.993C= MANE Select ENSP00000273951.8:p.Asn331=
ENST00000273951.12:c.993C= ENSP00000273951.8:p.Asn331=
ENST00000503472.5:n.877C=
ENST00000504199.5:c.1050C= ENSP00000421725.1:p.Asn350=
ENST00000509740.5:c.993C= ENSP00000422664.1:p.Asn331=
ENST00000513476.5:c.993C= ENSP00000426683.1:p.Asn331=
NM_000583.3:c.993C= NP_000574.2:p.Asn331=
NM_001204306.1:c.993C= NP_001191235.1:p.Asn331=
NM_001204307.1:c.1050C= NP_001191236.1:p.Asn350=
XM_006714177.2:c.993C= XP_006714240.1:p.Asn331=
XM_006714177.3:c.993C= XP_006714240.1:p.Asn331=
NM_000583.4:c.993C= MANE Select NP_000574.2:p.Asn331=