Canonical Allele Identifier: CA379562318

Gene: TUB

Linked Data

• dbSNP Id: rs2133832219
• MyVariant Identifiers: chr11:g.8111176A>G (hg19) ; chr11:g.8089629A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089629A>G , CM000673.2:g.8089629A>G	GRCh38
NC_000011.9:g.8111176A>G , CM000673.1:g.8111176A>G	GRCh37
NC_000011.8:g.8067752A>G	NCBI36
NG_029912.1:g.55997A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.58A>G MANE Select	ENSP00000299506.3:p.Arg20Gly
ENST00000299506.2:c.58A>G	ENSP00000299506.2:p.Arg20Gly
ENST00000305253.8:c.223A>G	ENSP00000305426.4:p.Arg75Gly
ENST00000534099.5:c.76A>G	ENSP00000434400.1:p.Arg26Gly
NM_003320.4:c.223A>G	NP_003311.2:p.Arg75Gly
NM_177972.2:c.58A>G	NP_813977.1:p.Arg20Gly
XM_005253109.2:c.184A>G	XP_005253166.1:p.Arg62Gly
XM_011520344.1:c.94A>G	XP_011518646.1:p.Arg32Gly
XM_005253109.3:c.184A>G	XP_005253166.1:p.Arg62Gly
XM_011520344.2:c.94A>G	XP_011518646.1:p.Arg32Gly
NM_177972.3:c.58A>G MANE Select	NP_813977.1:p.Arg20Gly
NM_003320.5:c.223A>G	NP_003311.2:p.Arg75Gly