Canonical Allele Identifier: CA2082357964

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317679G= , CM000675.2:g.31317679G=	GRCh38
NC_000013.10:g.31891816G= , CM000675.1:g.31891816G=	GRCh37
NC_000013.9:g.30789816G=	NCBI36
NG_011732.1:g.122705G=
NG_011732.2:g.122705G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343307.5:c.1178G= MANE Select	ENSP00000343002.4:p.Gly393=
ENST00000343307.4:c.1178G=	ENSP00000343002.4:p.Gly393=
NM_194318.3:c.1178G=	NP_919299.3:p.Gly393=
XM_006719768.2:c.1121G=	XP_006719831.1:p.Gly374=
XM_011534936.1:c.1065-6072G=	XP_011533238.1:n.1065-6072G=
XM_011534937.1:c.1058G=	XP_011533239.1:p.Gly353=
XM_011534938.1:c.1031G=	XP_011533240.1:p.Gly344=
XM_006719768.3:c.1121G=	XP_006719831.1:p.Gly374=
XM_011534938.2:c.1031G=	XP_011533240.1:p.Gly344=
XM_017020395.1:c.1031G=	XP_016875884.1:p.Gly344=
NM_194318.4:c.1178G= MANE Select	NP_919299.3:p.Gly393=