Canonical Allele Identifier: CA1457431785

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033596A= , CM000666.2:g.52033596A=	GRCh38
NC_000004.11:g.52899762A= , CM000666.1:g.52899762A=	GRCh37
NC_000004.10:g.52594519A=	NCBI36
NG_008891.1:g.9724T= , LRG_204:g.9724T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.78T= MANE Select	ENSP00000370839.6:p.Ala26=
ENST00000381431.9:c.78T=	ENSP00000370839.5:p.Ala26=
ENST00000506357.5:c.64T=
ENST00000514133.1:c.45T=	ENSP00000425818.1:p.Ala15=
NM_000232.4:c.78T= , LRG_204t1:c.78T=	NP_000223.1:p.Ala26=
XM_011534403.1:c.34-3733T=	XP_011532705.1:n.34-3733T=
NM_000232.5:c.78T= MANE Select	NP_000223.1:p.Ala26=