Canonical Allele Identifier: CA1457429990

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029766G= , CM000666.2:g.52029766G=	GRCh38
NC_000004.11:g.52895932G= , CM000666.1:g.52895932G=	GRCh37
NC_000004.10:g.52590689G=	NCBI36
NG_008891.1:g.13554C= , LRG_204:g.13554C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.341C= MANE Select	ENSP00000370839.6:p.Ser114=
ENST00000381431.9:c.341C=	ENSP00000370839.5:p.Ser114=
ENST00000506357.5:c.424C=
ENST00000514133.1:c.418C=	ENSP00000425818.1:n.418C=
NM_000232.4:c.341C= , LRG_204t1:c.341C=	NP_000223.1:p.Ser114=
XM_006714049.2:c.44C=	XP_006714112.1:p.Ser15=
XM_011534403.1:c.131C=	XP_011532705.1:p.Ser44=
XM_011534404.1:c.44C=	XP_011532706.1:p.Ser15=
NM_000232.5:c.341C= MANE Select	NP_000223.1:p.Ser114=