Canonical Allele Identifier: CA9301187
Gene: B3GNT3 HGNC NCBI

Linked Data

dbSNP Id: rs36686

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17811986G>A , CM000681.2:g.17811986G>A GRCh38
NC_000019.9:g.17922795G>A , CM000681.1:g.17922795G>A GRCh37
NC_000019.8:g.17783795G>A NCBI36
NG_028981.1:g.21877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318683.7:c.983G>A MANE Select ENSP00000321874.5:p.Arg328His
ENST00000318683.6:c.983G>A ENSP00000321874.5:p.Arg328His
ENST00000595387.1:c.983G>A ENSP00000472638.1:p.Arg328His
NM_014256.3:c.983G>A NP_055071.2:p.Arg328His
XM_011527626.1:c.983G>A XP_011525928.1:p.Arg328His
XM_011527627.1:c.983G>A XP_011525929.1:p.Arg328His
XM_011527626.2:c.983G>A XP_011525928.1:p.Arg328His
NM_014256.4:c.983G>A MANE Select NP_055071.2:p.Arg328His