Canonical Allele Identifier: CA217414815

Gene: TUB

Linked Data

• dbSNP Id: rs907352524
• gnomAD v3: 11-8089413-A-G
• gnomAD v4: 11-8089413-A-G
• MyVariant Identifiers: chr11:g.8110960A>G (hg19) ; chr11:g.8089413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089413A>G , CM000673.2:g.8089413A>G	GRCh38
NC_000011.9:g.8110960A>G , CM000673.1:g.8110960A>G	GRCh37
NC_000011.8:g.8067536A>G	NCBI36
NG_029912.1:g.55781A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-197A>G MANE Select	ENSP00000299506.3:n.39-197A>G
ENST00000299506.2:c.39-197A>G	ENSP00000299506.2:n.39-197A>G
ENST00000305253.8:c.204-197A>G	ENSP00000305426.4:n.204-197A>G
ENST00000534099.5:c.57-197A>G	ENSP00000434400.1:n.57-197A>G
NM_003320.4:c.204-197A>G	NP_003311.2:n.204-197A>G
NM_177972.2:c.39-197A>G	NP_813977.1:n.39-197A>G
XM_005253109.2:c.165-197A>G	XP_005253166.1:n.165-197A>G
XM_011520344.1:c.75-197A>G	XP_011518646.1:n.75-197A>G
XM_005253109.3:c.165-197A>G	XP_005253166.1:n.165-197A>G
XM_011520344.2:c.75-197A>G	XP_011518646.1:n.75-197A>G
NM_177972.3:c.39-197A>G MANE Select	NP_813977.1:n.39-197A>G
NM_003320.5:c.204-197A>G	NP_003311.2:n.204-197A>G