Canonical Allele Identifier: CA1457429152

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028053C= , CM000666.2:g.52028053C=	GRCh38
NC_000004.11:g.52894219C= , CM000666.1:g.52894219C=	GRCh37
NC_000004.10:g.52588976C=	NCBI36
NG_008891.1:g.15267G= , LRG_204:g.15267G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.668G= MANE Select	ENSP00000370839.6:p.Arg223=
ENST00000381431.9:c.668G=	ENSP00000370839.5:p.Arg223=
NM_000232.4:c.668G= , LRG_204t1:c.668G=	NP_000223.1:p.Arg223=
XM_006714049.2:c.371G=	XP_006714112.1:p.Arg124=
XM_011534403.1:c.458G=	XP_011532705.1:p.Arg153=
XM_011534404.1:c.371G=	XP_011532706.1:p.Arg124=
NM_000232.5:c.668G= MANE Select	NP_000223.1:p.Arg223=