Canonical Allele Identifier: CA1457429996

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029783A= , CM000666.2:g.52029783A=	GRCh38
NC_000004.11:g.52895949A= , CM000666.1:g.52895949A=	GRCh37
NC_000004.10:g.52590706A=	NCBI36
NG_008891.1:g.13537T= , LRG_204:g.13537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.324T= MANE Select	ENSP00000370839.6:p.Leu108=
ENST00000381431.9:c.324T=	ENSP00000370839.5:p.Leu108=
ENST00000506357.5:c.407T=
ENST00000514133.1:c.401T=	ENSP00000425818.1:n.401T=
NM_000232.4:c.324T= , LRG_204t1:c.324T=	NP_000223.1:p.Leu108=
XM_006714049.2:c.27T=	XP_006714112.1:p.Leu9=
XM_011534403.1:c.114T=	XP_011532705.1:p.Leu38=
XM_011534404.1:c.27T=	XP_011532706.1:p.Leu9=
NM_000232.5:c.324T= MANE Select	NP_000223.1:p.Leu108=