Canonical Allele Identifier: CA6936835
Gene: B3GLCT HGNC NCBI

Linked Data

dbSNP Id: rs140760538

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31317682G>A , CM000675.2:g.31317682G>A GRCh38
NC_000013.10:g.31891819G>A , CM000675.1:g.31891819G>A GRCh37
NC_000013.9:g.30789819G>A NCBI36
NG_011732.1:g.122708G>A
NG_011732.2:g.122708G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343307.5:c.1181G>A MANE Select ENSP00000343002.4:p.Gly394Glu
ENST00000343307.4:c.1181G>A ENSP00000343002.4:p.Gly394Glu
NM_194318.3:c.1181G>A NP_919299.3:p.Gly394Glu
XM_006719768.2:c.1124G>A XP_006719831.1:p.Gly375Glu
XM_011534936.1:c.1065-6069G>A XP_011533238.1:n.1065-6069G>A
XM_011534937.1:c.1061G>A XP_011533239.1:p.Gly354Glu
XM_011534938.1:c.1034G>A XP_011533240.1:p.Gly345Glu
XM_006719768.3:c.1124G>A XP_006719831.1:p.Gly375Glu
XM_011534938.2:c.1034G>A XP_011533240.1:p.Gly345Glu
XM_017020395.1:c.1034G>A XP_016875884.1:p.Gly345Glu
NM_194318.4:c.1181G>A MANE Select NP_919299.3:p.Gly394Glu