Canonical Allele Identifier: CA1467373188
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71756755T= , CM000666.2:g.71756755T= GRCh38
NC_000004.11:g.72622472T= , CM000666.1:g.72622472T= GRCh37
NC_000004.10:g.72841336T= NCBI36
NG_012837.2:g.53766A=
NG_012837.3:g.53766A=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.991A= MANE Select ENSP00000273951.8:p.Asn331=
ENST00000273951.12:c.991A= ENSP00000273951.8:p.Asn331=
ENST00000503472.5:n.875A=
ENST00000504199.5:c.1048A= ENSP00000421725.1:p.Asn350=
ENST00000509740.5:c.991A= ENSP00000422664.1:p.Asn331=
ENST00000513476.5:c.991A= ENSP00000426683.1:p.Asn331=
NM_000583.3:c.991A= NP_000574.2:p.Asn331=
NM_001204306.1:c.991A= NP_001191235.1:p.Asn331=
NM_001204307.1:c.1048A= NP_001191236.1:p.Asn350=
XM_006714177.2:c.991A= XP_006714240.1:p.Asn331=
XM_006714177.3:c.991A= XP_006714240.1:p.Asn331=
NM_000583.4:c.991A= MANE Select NP_000574.2:p.Asn331=