Canonical Allele Identifier: CA680747108
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1180587512
gnomAD v3: 11-8089900-G-A
gnomAD v4: 11-8089900-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089900G>A , CM000673.2:g.8089900G>A GRCh38
NC_000011.9:g.8111447G>A , CM000673.1:g.8111447G>A GRCh37
NC_000011.8:g.8068023G>A NCBI36
NG_029912.1:g.56268G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-169G>A MANE Select ENSP00000299506.3:n.91-169G>A
ENST00000299506.2:c.91-169G>A ENSP00000299506.2:n.91-169G>A
ENST00000305253.8:c.256-169G>A ENSP00000305426.4:n.256-169G>A
ENST00000534099.5:c.109-169G>A ENSP00000434400.1:n.109-169G>A
NM_003320.4:c.256-169G>A NP_003311.2:n.256-169G>A
NM_177972.2:c.91-169G>A NP_813977.1:n.91-169G>A
XM_005253109.2:c.217-169G>A XP_005253166.1:n.217-169G>A
XM_011520344.1:c.127-169G>A XP_011518646.1:n.127-169G>A
XM_005253109.3:c.217-169G>A XP_005253166.1:n.217-169G>A
XM_011520344.2:c.127-169G>A XP_011518646.1:n.127-169G>A
NM_177972.3:c.91-169G>A MANE Select NP_813977.1:n.91-169G>A
NM_003320.5:c.256-169G>A NP_003311.2:n.256-169G>A