Canonical Allele Identifier: CA1467352528
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71748580T= , CM000666.2:g.71748580T= GRCh38
NC_000004.11:g.72614297T= , CM000666.1:g.72614297T= GRCh37
NC_000004.10:g.72833161T= NCBI36
NG_012837.2:g.61941A=
NG_012837.3:g.61941A=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1396-2375A= MANE Select ENSP00000273951.8:n.1396-2375A=
ENST00000273951.12:c.1396-2375A= ENSP00000273951.8:n.1396-2375A=
ENST00000503364.5:n.69-2375A=
ENST00000503472.5:n.1280-2375A=
ENST00000504199.5:c.1453-2375A= ENSP00000421725.1:n.1453-2375A=
ENST00000509740.5:c.*219-2375A= ENSP00000422664.1:n.*219-2375A=
ENST00000513476.5:c.1395+3938A= ENSP00000426683.1:n.1395+3938A=
NM_000583.3:c.1396-2375A= NP_000574.2:n.1396-2375A=
NM_001204306.1:c.1396-2375A= NP_001191235.1:n.1396-2375A=
NM_001204307.1:c.1453-2375A= NP_001191236.1:n.1453-2375A=
XM_006714177.2:c.1263-2375A= XP_006714240.1:n.1263-2375A=
XM_006714177.3:c.1263-2375A= XP_006714240.1:n.1263-2375A=
NM_000583.4:c.1396-2375A= MANE Select NP_000574.2:n.1396-2375A=