Canonical Allele Identifier: CA1457429946

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029683G= , CM000666.2:g.52029683G=	GRCh38
NC_000004.11:g.52895849G= , CM000666.1:g.52895849G=	GRCh37
NC_000004.10:g.52590606G=	NCBI36
NG_008891.1:g.13637C= , LRG_204:g.13637C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.424C= MANE Select	ENSP00000370839.6:p.Gln142=
ENST00000381431.9:c.424C=	ENSP00000370839.5:p.Gln142=
ENST00000506357.5:c.507C=
ENST00000514133.1:c.501C=	ENSP00000425818.1:n.501C=
NM_000232.4:c.424C= , LRG_204t1:c.424C=	NP_000223.1:p.Gln142=
XM_006714049.2:c.127C=	XP_006714112.1:p.Gln43=
XM_011534403.1:c.214C=	XP_011532705.1:p.Gln72=
XM_011534404.1:c.127C=	XP_011532706.1:p.Gln43=
NM_000232.5:c.424C= MANE Select	NP_000223.1:p.Gln142=