Canonical Allele Identifier: CA1457429991

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029773G= , CM000666.2:g.52029773G=	GRCh38
NC_000004.11:g.52895939G= , CM000666.1:g.52895939G=	GRCh37
NC_000004.10:g.52590696G=	NCBI36
NG_008891.1:g.13547C= , LRG_204:g.13547C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.334C= MANE Select	ENSP00000370839.6:p.Gln112=
ENST00000381431.9:c.334C=	ENSP00000370839.5:p.Gln112=
ENST00000506357.5:c.417C=
ENST00000514133.1:c.411C=	ENSP00000425818.1:n.411C=
NM_000232.4:c.334C= , LRG_204t1:c.334C=	NP_000223.1:p.Gln112=
XM_006714049.2:c.37C=	XP_006714112.1:p.Gln13=
XM_011534403.1:c.124C=	XP_011532705.1:p.Gln42=
XM_011534404.1:c.37C=	XP_011532706.1:p.Gln13=
NM_000232.5:c.334C= MANE Select	NP_000223.1:p.Gln112=