Canonical Allele Identifier: CA2082318224

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31269250C= , CM000675.2:g.31269250C=	GRCh38
NC_000013.10:g.31843387C= , CM000675.1:g.31843387C=	GRCh37
NC_000013.9:g.30741387C=	NCBI36
NG_011732.1:g.74276C=
NG_011732.2:g.74276C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.633C= MANE Select	ENSP00000343002.4:p.Ser211=
ENST00000343307.4:c.633C=	ENSP00000343002.4:p.Ser211=
ENST00000461652.2:n.248C=
NM_194318.3:c.633C=	NP_919299.3:p.Ser211=
XM_006719768.2:c.576C=	XP_006719831.1:p.Ser192=
XM_011534936.1:c.633C=	XP_011533238.1:p.Ser211=
XM_011534937.1:c.633C=	XP_011533239.1:p.Ser211=
XM_011534938.1:c.486C=	XP_011533240.1:p.Ser162=
XR_941500.1:n.732C=
XR_941501.1:n.732C=
XM_006719768.3:c.576C=	XP_006719831.1:p.Ser192=
XM_011534938.2:c.486C=	XP_011533240.1:p.Ser162=
XM_017020395.1:c.486C=	XP_016875884.1:p.Ser162=
NM_194318.4:c.633C= MANE Select	NP_919299.3:p.Ser211=