Canonical Allele Identifier: CA934888148
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1943737938

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089863G>A , CM000673.2:g.8089863G>A GRCh38
NC_000011.9:g.8111410G>A , CM000673.1:g.8111410G>A GRCh37
NC_000011.8:g.8067986G>A NCBI36
NG_029912.1:g.56231G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.90+202G>A MANE Select ENSP00000299506.3:n.90+202G>A
ENST00000299506.2:c.90+202G>A ENSP00000299506.2:n.90+202G>A
ENST00000305253.8:c.255+202G>A ENSP00000305426.4:n.255+202G>A
ENST00000534099.5:c.108+202G>A ENSP00000434400.1:n.108+202G>A
NM_003320.4:c.255+202G>A NP_003311.2:n.255+202G>A
NM_177972.2:c.90+202G>A NP_813977.1:n.90+202G>A
XM_005253109.2:c.216+202G>A XP_005253166.1:n.216+202G>A
XM_011520344.1:c.126+202G>A XP_011518646.1:n.126+202G>A
XM_005253109.3:c.216+202G>A XP_005253166.1:n.216+202G>A
XM_011520344.2:c.126+202G>A XP_011518646.1:n.126+202G>A
NM_177972.3:c.90+202G>A MANE Select NP_813977.1:n.90+202G>A
NM_003320.5:c.255+202G>A NP_003311.2:n.255+202G>A