Canonical Allele Identifier: CA680747129
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1318166494
gnomAD v4: 11-8089935-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089935T>C , CM000673.2:g.8089935T>C GRCh38
NC_000011.9:g.8111482T>C , CM000673.1:g.8111482T>C GRCh37
NC_000011.8:g.8068058T>C NCBI36
NG_029912.1:g.56303T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-134T>C MANE Select ENSP00000299506.3:n.91-134T>C
ENST00000299506.2:c.91-134T>C ENSP00000299506.2:n.91-134T>C
ENST00000305253.8:c.256-134T>C ENSP00000305426.4:n.256-134T>C
ENST00000534099.5:c.109-134T>C ENSP00000434400.1:n.109-134T>C
NM_003320.4:c.256-134T>C NP_003311.2:n.256-134T>C
NM_177972.2:c.91-134T>C NP_813977.1:n.91-134T>C
XM_005253109.2:c.217-134T>C XP_005253166.1:n.217-134T>C
XM_011520344.1:c.127-134T>C XP_011518646.1:n.127-134T>C
XM_005253109.3:c.217-134T>C XP_005253166.1:n.217-134T>C
XM_011520344.2:c.127-134T>C XP_011518646.1:n.127-134T>C
NM_177972.3:c.91-134T>C MANE Select NP_813977.1:n.91-134T>C
NM_003320.5:c.256-134T>C NP_003311.2:n.256-134T>C