Canonical Allele Identifier: CA2082357670

Gene: B3GLCT

Linked Data

• dbSNP Id: rs1875103334

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.31317513A>C , CM000675.2:g.31317513A>C	GRCh38
NC_000013.10:g.31891650A>C , CM000675.1:g.31891650A>C	GRCh37
NC_000013.9:g.30789650A>C	NCBI36
NG_011732.1:g.122539A>C
NG_011732.2:g.122539A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343307.5:c.1065-53A>C MANE Select	ENSP00000343002.4:n.1065-53A>C
ENST00000343307.4:c.1065-53A>C	ENSP00000343002.4:n.1065-53A>C
NM_194318.3:c.1065-53A>C	NP_919299.3:n.1065-53A>C
XM_006719768.2:c.1008-53A>C	XP_006719831.1:n.1008-53A>C
XM_011534936.1:c.1065-6238A>C	XP_011533238.1:n.1065-6238A>C
XM_011534937.1:c.945-53A>C	XP_011533239.1:n.945-53A>C
XM_011534938.1:c.918-53A>C	XP_011533240.1:n.918-53A>C
XR_941500.1:n.1250-53A>C
XR_941501.1:n.1130-53A>C
XM_006719768.3:c.1008-53A>C	XP_006719831.1:n.1008-53A>C
XM_011534938.2:c.918-53A>C	XP_011533240.1:n.918-53A>C
XM_017020395.1:c.918-53A>C	XP_016875884.1:n.918-53A>C
NM_194318.4:c.1065-53A>C MANE Select	NP_919299.3:n.1065-53A>C