Canonical Allele Identifier: CA1457429993

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029780T= , CM000666.2:g.52029780T=	GRCh38
NC_000004.11:g.52895946T= , CM000666.1:g.52895946T=	GRCh37
NC_000004.10:g.52590703T=	NCBI36
NG_008891.1:g.13540A= , LRG_204:g.13540A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.327A= MANE Select	ENSP00000370839.6:p.Arg109=
ENST00000381431.9:c.327A=	ENSP00000370839.5:p.Arg109=
ENST00000506357.5:c.410A=
ENST00000514133.1:c.404A=	ENSP00000425818.1:n.404A=
NM_000232.4:c.327A= , LRG_204t1:c.327A=	NP_000223.1:p.Arg109=
XM_006714049.2:c.30A=	XP_006714112.1:p.Arg10=
XM_011534403.1:c.117A=	XP_011532705.1:p.Arg39=
XM_011534404.1:c.30A=	XP_011532706.1:p.Arg10=
NM_000232.5:c.327A= MANE Select	NP_000223.1:p.Arg109=