Canonical Allele Identifier: CA1457429128

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028002T= , CM000666.2:g.52028002T=	GRCh38
NC_000004.11:g.52894168T= , CM000666.1:g.52894168T=	GRCh37
NC_000004.10:g.52588925T=	NCBI36
NG_008891.1:g.15318A= , LRG_204:g.15318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.719A= MANE Select	ENSP00000370839.6:p.Glu240=
ENST00000381431.9:c.719A=	ENSP00000370839.5:p.Glu240=
NM_000232.4:c.719A= , LRG_204t1:c.719A=	NP_000223.1:p.Glu240=
XM_006714049.2:c.422A=	XP_006714112.1:p.Glu141=
XM_011534403.1:c.509A=	XP_011532705.1:p.Glu170=
XM_011534404.1:c.422A=	XP_011532706.1:p.Glu141=
NM_000232.5:c.719A= MANE Select	NP_000223.1:p.Glu240=