Canonical Allele Identifier: CA1457431786

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033598C= , CM000666.2:g.52033598C=	GRCh38
NC_000004.11:g.52899764C= , CM000666.1:g.52899764C=	GRCh37
NC_000004.10:g.52594521C=	NCBI36
NG_008891.1:g.9722G= , LRG_204:g.9722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.76G= MANE Select	ENSP00000370839.6:p.Ala26=
ENST00000381431.9:c.76G=	ENSP00000370839.5:p.Ala26=
ENST00000506357.5:c.62G=
ENST00000514133.1:c.43G=	ENSP00000425818.1:p.Ala15=
NM_000232.4:c.76G= , LRG_204t1:c.76G=	NP_000223.1:p.Ala26=
XM_011534403.1:c.34-3735G=	XP_011532705.1:n.34-3735G=
NM_000232.5:c.76G= MANE Select	NP_000223.1:p.Ala26=