Canonical Allele Identifier: CA387819189
Gene: B3GLCT HGNC NCBI

Linked Data

dbSNP Id: rs1413640266

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31317684G>T , CM000675.2:g.31317684G>T GRCh38
NC_000013.10:g.31891821G>T , CM000675.1:g.31891821G>T GRCh37
NC_000013.9:g.30789821G>T NCBI36
NG_011732.1:g.122710G>T
NG_011732.2:g.122710G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343307.5:c.1183G>T MANE Select ENSP00000343002.4:p.Gly395Ter
ENST00000343307.4:c.1183G>T ENSP00000343002.4:p.Gly395Ter
NM_194318.3:c.1183G>T NP_919299.3:p.Gly395Ter
XM_006719768.2:c.1126G>T XP_006719831.1:p.Gly376Ter
XM_011534936.1:c.1065-6067G>T XP_011533238.1:n.1065-6067G>T
XM_011534937.1:c.1063G>T XP_011533239.1:p.Gly355Ter
XM_011534938.1:c.1036G>T XP_011533240.1:p.Gly346Ter
XM_006719768.3:c.1126G>T XP_006719831.1:p.Gly376Ter
XM_011534938.2:c.1036G>T XP_011533240.1:p.Gly346Ter
XM_017020395.1:c.1036G>T XP_016875884.1:p.Gly346Ter
NM_194318.4:c.1183G>T MANE Select NP_919299.3:p.Gly395Ter