Canonical Allele Identifier: CA2082357678

Gene: B3GLCT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317517C= , CM000675.2:g.31317517C=	GRCh38
NC_000013.10:g.31891654C= , CM000675.1:g.31891654C=	GRCh37
NC_000013.9:g.30789654C=	NCBI36
NG_011732.1:g.122543C=
NG_011732.2:g.122543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343307.5:c.1065-49C= MANE Select	ENSP00000343002.4:n.1065-49C=
ENST00000343307.4:c.1065-49C=	ENSP00000343002.4:n.1065-49C=
NM_194318.3:c.1065-49C=	NP_919299.3:n.1065-49C=
XM_006719768.2:c.1008-49C=	XP_006719831.1:n.1008-49C=
XM_011534936.1:c.1065-6234C=	XP_011533238.1:n.1065-6234C=
XM_011534937.1:c.945-49C=	XP_011533239.1:n.945-49C=
XM_011534938.1:c.918-49C=	XP_011533240.1:n.918-49C=
XR_941500.1:n.1250-49C=
XR_941501.1:n.1130-49C=
XM_006719768.3:c.1008-49C=	XP_006719831.1:n.1008-49C=
XM_011534938.2:c.918-49C=	XP_011533240.1:n.918-49C=
XM_017020395.1:c.918-49C=	XP_016875884.1:n.918-49C=
NM_194318.4:c.1065-49C= MANE Select	NP_919299.3:n.1065-49C=