Canonical Allele Identifier: CA1457429000

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027739G= , CM000666.2:g.52027739G=	GRCh38
NC_000004.11:g.52893905G= , CM000666.1:g.52893905G=	GRCh37
NC_000004.10:g.52588662G=	NCBI36
NG_008891.1:g.15581C= , LRG_204:g.15581C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.753+229C= MANE Select	ENSP00000370839.6:n.753+229C=
ENST00000381431.9:c.753+229C=	ENSP00000370839.5:n.753+229C=
NM_000232.4:c.753+229C= , LRG_204t1:c.753+229C=	NP_000223.1:n.753+229C=
XM_006714049.2:c.456+229C=	XP_006714112.1:n.456+229C=
XM_011534403.1:c.543+229C=	XP_011532705.1:n.543+229C=
XM_011534404.1:c.456+229C=	XP_011532706.1:n.456+229C=
NM_000232.5:c.753+229C= MANE Select	NP_000223.1:n.753+229C=