Canonical Allele Identifier: CA1467385586
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71783965C= , CM000666.2:g.71783965C= GRCh38
NC_000004.11:g.72649682C= , CM000666.1:g.72649682C= GRCh37
NC_000004.10:g.72868546C= NCBI36
NG_012837.2:g.26556G=
NG_012837.3:g.26556G=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.54G= MANE Select ENSP00000273951.8:p.Glu18=
ENST00000273951.12:c.54G= ENSP00000273951.8:p.Glu18=
ENST00000504199.5:c.111G= ENSP00000421725.1:p.Glu37=
ENST00000506245.1:c.54G= ENSP00000426718.1:p.Glu18=
ENST00000509740.5:c.54G= ENSP00000422664.1:p.Glu18=
ENST00000513476.5:c.54G= ENSP00000426683.1:p.Glu18=
NM_000583.3:c.54G= NP_000574.2:p.Glu18=
NM_001204306.1:c.54G= NP_001191235.1:p.Glu18=
NM_001204307.1:c.111G= NP_001191236.1:p.Glu37=
XM_006714177.2:c.54G= XP_006714240.1:p.Glu18=
XM_006714177.3:c.54G= XP_006714240.1:p.Glu18=
NM_000583.4:c.54G= MANE Select NP_000574.2:p.Glu18=