Canonical Allele Identifier: CA1457430008

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029817C= , CM000666.2:g.52029817C=	GRCh38
NC_000004.11:g.52895983C= , CM000666.1:g.52895983C=	GRCh37
NC_000004.10:g.52590740C=	NCBI36
NG_008891.1:g.13503G= , LRG_204:g.13503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.290G= MANE Select	ENSP00000370839.6:p.Cys97=
ENST00000381431.9:c.290G=	ENSP00000370839.5:p.Cys97=
ENST00000506357.5:c.373G=
ENST00000514133.1:c.367G=	ENSP00000425818.1:n.367G=
NM_000232.4:c.290G= , LRG_204t1:c.290G=	NP_000223.1:p.Cys97=
XM_006714049.2:c.-8G=	XP_006714112.1:n.-8G=
XM_011534403.1:c.80G=	XP_011532705.1:p.Cys27=
XM_011534404.1:c.-8G=	XP_011532706.1:n.-8G=
NM_000232.5:c.290G= MANE Select	NP_000223.1:p.Cys97=