Canonical Allele Identifier: CA1950952504
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1943728474

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089384C>T , CM000673.2:g.8089384C>T GRCh38
NC_000011.9:g.8110931C>T , CM000673.1:g.8110931C>T GRCh37
NC_000011.8:g.8067507C>T NCBI36
NG_029912.1:g.55752C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-226C>T MANE Select ENSP00000299506.3:n.39-226C>T
ENST00000299506.2:c.39-226C>T ENSP00000299506.2:n.39-226C>T
ENST00000305253.8:c.204-226C>T ENSP00000305426.4:n.204-226C>T
ENST00000534099.5:c.57-226C>T ENSP00000434400.1:n.57-226C>T
NM_003320.4:c.204-226C>T NP_003311.2:n.204-226C>T
NM_177972.2:c.39-226C>T NP_813977.1:n.39-226C>T
XM_005253109.2:c.165-226C>T XP_005253166.1:n.165-226C>T
XM_011520344.1:c.75-226C>T XP_011518646.1:n.75-226C>T
XM_005253109.3:c.165-226C>T XP_005253166.1:n.165-226C>T
XM_011520344.2:c.75-226C>T XP_011518646.1:n.75-226C>T
NM_177972.3:c.39-226C>T MANE Select NP_813977.1:n.39-226C>T
NM_003320.5:c.204-226C>T NP_003311.2:n.204-226C>T