Canonical Allele Identifier: CA1457429132

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028009T= , CM000666.2:g.52028009T=	GRCh38
NC_000004.11:g.52894175T= , CM000666.1:g.52894175T=	GRCh37
NC_000004.10:g.52588932T=	NCBI36
NG_008891.1:g.15311A= , LRG_204:g.15311A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.712A= MANE Select	ENSP00000370839.6:p.Thr238=
ENST00000381431.9:c.712A=	ENSP00000370839.5:p.Thr238=
NM_000232.4:c.712A= , LRG_204t1:c.712A=	NP_000223.1:p.Thr238=
XM_006714049.2:c.415A=	XP_006714112.1:p.Thr139=
XM_011534403.1:c.502A=	XP_011532705.1:p.Thr168=
XM_011534404.1:c.415A=	XP_011532706.1:p.Thr139=
NM_000232.5:c.712A= MANE Select	NP_000223.1:p.Thr238=