Canonical Allele Identifier: CA1457429021

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027777C= , CM000666.2:g.52027777C=	GRCh38
NC_000004.11:g.52893943C= , CM000666.1:g.52893943C=	GRCh37
NC_000004.10:g.52588700C=	NCBI36
NG_008891.1:g.15543G= , LRG_204:g.15543G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.753+191G= MANE Select	ENSP00000370839.6:n.753+191G=
ENST00000381431.9:c.753+191G=	ENSP00000370839.5:n.753+191G=
NM_000232.4:c.753+191G= , LRG_204t1:c.753+191G=	NP_000223.1:n.753+191G=
XM_006714049.2:c.456+191G=	XP_006714112.1:n.456+191G=
XM_011534403.1:c.543+191G=	XP_011532705.1:n.543+191G=
XM_011534404.1:c.456+191G=	XP_011532706.1:n.456+191G=
NM_000232.5:c.753+191G= MANE Select	NP_000223.1:n.753+191G=