Canonical Allele Identifier: CA2078590960

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23250610T= , CM000675.2:g.23250610T=	GRCh38
NC_000013.10:g.23824749T= , CM000675.1:g.23824749T=	GRCh37
NC_000013.9:g.22722749T=	NCBI36
NG_008759.1:g.74690T= , LRG_207:g.74690T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.298-20T= MANE Select	ENSP00000218867.3:n.298-20T=
ENST00000218867.3:c.298-20T=	ENSP00000218867.3:n.298-20T=
NM_000231.2:c.298-20T= , LRG_207t1:c.298-20T=	NP_000222.1:n.298-20T=
XM_005266505.2:c.298-20T=	XP_005266562.1:n.298-20T=
XM_006719861.2:c.352-20T=	XP_006719924.1:n.352-20T=
XM_006719861.3:c.352-20T=	XP_006719924.1:n.352-20T=
XM_024449397.1:c.298-20T=	XP_024305165.1:n.298-20T=
NM_000231.3:c.298-20T= MANE Select	NP_000222.2:n.298-20T=
NM_001378244.1:c.352-20T=	NP_001365173.1:n.352-20T=
NM_001378245.1:c.298-20T=	NP_001365174.1:n.298-20T=
NM_001378246.1:c.298-20T=	NP_001365175.1:n.298-20T=