Canonical Allele Identifier: CA217415395
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs957961900
gnomAD v4: 11-8090004-C-T
MyVariant Identifiers: chr11:g.8090004C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090004C>T , CM000673.2:g.8090004C>T GRCh38
NC_000011.9:g.8111551C>T , CM000673.1:g.8111551C>T GRCh37
NC_000011.8:g.8068127C>T NCBI36
NG_029912.1:g.56372C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-65C>T MANE Select ENSP00000299506.3:n.91-65C>T
ENST00000299506.2:c.91-65C>T ENSP00000299506.2:n.91-65C>T
ENST00000305253.8:c.256-65C>T ENSP00000305426.4:n.256-65C>T
ENST00000534099.5:c.109-65C>T ENSP00000434400.1:n.109-65C>T
NM_003320.4:c.256-65C>T NP_003311.2:n.256-65C>T
NM_177972.2:c.91-65C>T NP_813977.1:n.91-65C>T
XM_005253109.2:c.217-65C>T XP_005253166.1:n.217-65C>T
XM_011520344.1:c.127-65C>T XP_011518646.1:n.127-65C>T
XM_005253109.3:c.217-65C>T XP_005253166.1:n.217-65C>T
XM_011520344.2:c.127-65C>T XP_011518646.1:n.127-65C>T
NM_177972.3:c.91-65C>T MANE Select NP_813977.1:n.91-65C>T
NM_003320.5:c.256-65C>T NP_003311.2:n.256-65C>T