Canonical Allele Identifier: CA1457429143

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028029C= , CM000666.2:g.52028029C=	GRCh38
NC_000004.11:g.52894195C= , CM000666.1:g.52894195C=	GRCh37
NC_000004.10:g.52588952C=	NCBI36
NG_008891.1:g.15291G= , LRG_204:g.15291G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.692G= MANE Select	ENSP00000370839.6:p.Gly231=
ENST00000381431.9:c.692G=	ENSP00000370839.5:p.Gly231=
NM_000232.4:c.692G= , LRG_204t1:c.692G=	NP_000223.1:p.Gly231=
XM_006714049.2:c.395G=	XP_006714112.1:p.Gly132=
XM_011534403.1:c.482G=	XP_011532705.1:p.Gly161=
XM_011534404.1:c.395G=	XP_011532706.1:p.Gly132=
NM_000232.5:c.692G= MANE Select	NP_000223.1:p.Gly231=