Canonical Allele Identifier: CA1457429945

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029681C= , CM000666.2:g.52029681C=	GRCh38
NC_000004.11:g.52895847C= , CM000666.1:g.52895847C=	GRCh37
NC_000004.10:g.52590604C=	NCBI36
NG_008891.1:g.13639G= , LRG_204:g.13639G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.426G= MANE Select	ENSP00000370839.6:p.Gln142=
ENST00000381431.9:c.426G=	ENSP00000370839.5:p.Gln142=
ENST00000506357.5:c.509G=
ENST00000514133.1:c.503G=	ENSP00000425818.1:n.503G=
NM_000232.4:c.426G= , LRG_204t1:c.426G=	NP_000223.1:p.Gln142=
XM_006714049.2:c.129G=	XP_006714112.1:p.Gln43=
XM_011534403.1:c.216G=	XP_011532705.1:p.Gln72=
XM_011534404.1:c.129G=	XP_011532706.1:p.Gln43=
NM_000232.5:c.426G= MANE Select	NP_000223.1:p.Gln142=