Canonical Allele Identifier: CA1950953072
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1589961967

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089901C>G , CM000673.2:g.8089901C>G GRCh38
NC_000011.9:g.8111448C>G , CM000673.1:g.8111448C>G GRCh37
NC_000011.8:g.8068024C>G NCBI36
NG_029912.1:g.56269C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-168C>G MANE Select ENSP00000299506.3:n.91-168C>G
ENST00000299506.2:c.91-168C>G ENSP00000299506.2:n.91-168C>G
ENST00000305253.8:c.256-168C>G ENSP00000305426.4:n.256-168C>G
ENST00000534099.5:c.109-168C>G ENSP00000434400.1:n.109-168C>G
NM_003320.4:c.256-168C>G NP_003311.2:n.256-168C>G
NM_177972.2:c.91-168C>G NP_813977.1:n.91-168C>G
XM_005253109.2:c.217-168C>G XP_005253166.1:n.217-168C>G
XM_011520344.1:c.127-168C>G XP_011518646.1:n.127-168C>G
XM_005253109.3:c.217-168C>G XP_005253166.1:n.217-168C>G
XM_011520344.2:c.127-168C>G XP_011518646.1:n.127-168C>G
NM_177972.3:c.91-168C>G MANE Select NP_813977.1:n.91-168C>G
NM_003320.5:c.256-168C>G NP_003311.2:n.256-168C>G