Canonical Allele Identifier: CA1457431685

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52033360T= , CM000666.2:g.52033360T=	GRCh38
NC_000004.11:g.52899526T= , CM000666.1:g.52899526T=	GRCh37
NC_000004.10:g.52594283T=	NCBI36
NG_008891.1:g.9960A= , LRG_204:g.9960A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.243+71A= MANE Select	ENSP00000370839.6:n.243+71A=
ENST00000381431.9:c.243+71A=	ENSP00000370839.5:n.243+71A=
ENST00000506357.5:c.229+71A=
ENST00000514133.1:c.210+71A=	ENSP00000425818.1:n.210+71A=
NM_000232.4:c.243+71A= , LRG_204t1:c.243+71A=	NP_000223.1:n.243+71A=
XM_006714049.2:c.-165+71A=	XP_006714112.1:n.-165+71A=
XM_011534403.1:c.34-3497A=	XP_011532705.1:n.34-3497A=
XM_011534404.1:c.-142+71A=	XP_011532706.1:n.-142+71A=
NM_000232.5:c.243+71A= MANE Select	NP_000223.1:n.243+71A=