Canonical Allele Identifier: CA473009112
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1943745404
MyVariant Identifiers: chr11:g.8111735G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090188G>A , CM000673.2:g.8090188G>A GRCh38
NC_000011.9:g.8111735G>A , CM000673.1:g.8111735G>A GRCh37
NC_000011.8:g.8068311G>A NCBI36
NG_029912.1:g.56556G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.210G>A MANE Select ENSP00000299506.3:p.Leu70=
ENST00000299506.2:c.210G>A ENSP00000299506.2:p.Leu70=
ENST00000305253.8:c.375G>A ENSP00000305426.4:p.Leu125=
ENST00000534099.5:c.228G>A ENSP00000434400.1:p.Leu76=
NM_003320.4:c.375G>A NP_003311.2:p.Leu125=
NM_177972.2:c.210G>A NP_813977.1:p.Leu70=
XM_005253109.2:c.336G>A XP_005253166.1:p.Leu112=
XM_011520344.1:c.246G>A XP_011518646.1:p.Leu82=
XM_005253109.3:c.336G>A XP_005253166.1:p.Leu112=
XM_011520344.2:c.246G>A XP_011518646.1:p.Leu82=
NM_177972.3:c.210G>A MANE Select NP_813977.1:p.Leu70=
NM_003320.5:c.375G>A NP_003311.2:p.Leu125=