Canonical Allele Identifier: CA1467372809
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71755878C= , CM000666.2:g.71755878C= GRCh38
NC_000004.11:g.72621595C= , CM000666.1:g.72621595C= GRCh37
NC_000004.10:g.72840459C= NCBI36
NG_012837.2:g.54643G=
NG_012837.3:g.54643G=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1035-771G= MANE Select ENSP00000273951.8:n.1035-771G=
ENST00000273951.12:c.1035-771G= ENSP00000273951.8:n.1035-771G=
ENST00000503472.5:n.919-771G=
ENST00000504199.5:c.1092-771G= ENSP00000421725.1:n.1092-771G=
ENST00000509740.5:c.1034+834G= ENSP00000422664.1:n.1034+834G=
ENST00000513476.5:c.1035-771G= ENSP00000426683.1:n.1035-771G=
NM_000583.3:c.1035-771G= NP_000574.2:n.1035-771G=
NM_001204306.1:c.1035-771G= NP_001191235.1:n.1035-771G=
NM_001204307.1:c.1092-771G= NP_001191236.1:n.1092-771G=
XM_006714177.2:c.1035-771G= XP_006714240.1:n.1035-771G=
XM_006714177.3:c.1035-771G= XP_006714240.1:n.1035-771G=
NM_000583.4:c.1035-771G= MANE Select NP_000574.2:n.1035-771G=