Canonical Allele Identifier: CA2082318138

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31269181G= , CM000675.2:g.31269181G=	GRCh38
NC_000013.10:g.31843318G= , CM000675.1:g.31843318G=	GRCh37
NC_000013.9:g.30741318G=	NCBI36
NG_011732.1:g.74207G=
NG_011732.2:g.74207G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.597-33G= MANE Select	ENSP00000343002.4:n.597-33G=
ENST00000343307.4:c.597-33G=	ENSP00000343002.4:n.597-33G=
ENST00000461652.2:n.212-33G=
NM_194318.3:c.597-33G=	NP_919299.3:n.597-33G=
XM_006719768.2:c.540-33G=	XP_006719831.1:n.540-33G=
XM_011534936.1:c.597-33G=	XP_011533238.1:n.597-33G=
XM_011534937.1:c.597-33G=	XP_011533239.1:n.597-33G=
XM_011534938.1:c.450-33G=	XP_011533240.1:n.450-33G=
XR_941500.1:n.696-33G=
XR_941501.1:n.696-33G=
XM_006719768.3:c.540-33G=	XP_006719831.1:n.540-33G=
XM_011534938.2:c.450-33G=	XP_011533240.1:n.450-33G=
XM_017020395.1:c.450-33G=	XP_016875884.1:n.450-33G=
NM_194318.4:c.597-33G= MANE Select	NP_919299.3:n.597-33G=