Canonical Allele Identifier: CA1457430000

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029793C= , CM000666.2:g.52029793C=	GRCh38
NC_000004.11:g.52895959C= , CM000666.1:g.52895959C=	GRCh37
NC_000004.10:g.52590716C=	NCBI36
NG_008891.1:g.13527G= , LRG_204:g.13527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.314G= MANE Select	ENSP00000370839.6:p.Ser105=
ENST00000381431.9:c.314G=	ENSP00000370839.5:p.Ser105=
ENST00000506357.5:c.397G=
ENST00000514133.1:c.391G=	ENSP00000425818.1:n.391G=
NM_000232.4:c.314G= , LRG_204t1:c.314G=	NP_000223.1:p.Ser105=
XM_006714049.2:c.17G=	XP_006714112.1:p.Ser6=
XM_011534403.1:c.104G=	XP_011532705.1:p.Ser35=
XM_011534404.1:c.17G=	XP_011532706.1:p.Ser6=
NM_000232.5:c.314G= MANE Select	NP_000223.1:p.Ser105=