Canonical Allele Identifier: CA1950953035
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs550655039

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089848C>G , CM000673.2:g.8089848C>G GRCh38
NC_000011.9:g.8111395C>G , CM000673.1:g.8111395C>G GRCh37
NC_000011.8:g.8067971C>G NCBI36
NG_029912.1:g.56216C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.90+187C>G MANE Select ENSP00000299506.3:n.90+187C>G
ENST00000299506.2:c.90+187C>G ENSP00000299506.2:n.90+187C>G
ENST00000305253.8:c.255+187C>G ENSP00000305426.4:n.255+187C>G
ENST00000534099.5:c.108+187C>G ENSP00000434400.1:n.108+187C>G
NM_003320.4:c.255+187C>G NP_003311.2:n.255+187C>G
NM_177972.2:c.90+187C>G NP_813977.1:n.90+187C>G
XM_005253109.2:c.216+187C>G XP_005253166.1:n.216+187C>G
XM_011520344.1:c.126+187C>G XP_011518646.1:n.126+187C>G
XM_005253109.3:c.216+187C>G XP_005253166.1:n.216+187C>G
XM_011520344.2:c.126+187C>G XP_011518646.1:n.126+187C>G
NM_177972.3:c.90+187C>G MANE Select NP_813977.1:n.90+187C>G
NM_003320.5:c.255+187C>G NP_003311.2:n.255+187C>G