Canonical Allele Identifier: CA449777161
Gene: TUBB HGNC NCBI

Linked Data

dbSNP Id: rs1776473500
gnomAD v4: 6-30724268-C-T
MyVariant Identifiers: chr6:g.30692045C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724268C>T , CM000668.2:g.30724268C>T GRCh38
NC_000006.11:g.30692045C>T , CM000668.1:g.30692045C>T GRCh37
NC_000006.10:g.30800024C>T NCBI36
NG_034142.1:g.9068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1206C>T MANE Select ENSP00000339001.7:p.Gly402=
ENST00000680530.1:n.2068C>T
ENST00000681421.1:n.2272C>T
ENST00000681435.1:c.990C>T ENSP00000506665.1:p.Gly330=
ENST00000327892.12:c.1206C>T ENSP00000339001.7:p.Gly402=
ENST00000330914.7:c.990C>T ENSP00000365578.2:p.Gly330=
ENST00000396384.1:c.990C>T ENSP00000379668.1:p.Gly330=
ENST00000396389.5:c.1152C>T ENSP00000379672.1:p.Gly384=
NM_001293212.1:c.1266C>T NP_001280141.1:p.Gly422=
NM_001293213.1:c.600C>T NP_001280142.1:p.Gly200=
NM_001293214.1:c.1074C>T NP_001280143.1:p.Gly358=
NM_001293215.1:c.990C>T NP_001280144.1:p.Gly330=
NM_001293216.1:c.990C>T NP_001280145.1:p.Gly330=
NM_178014.3:c.1206C>T NP_821133.1:p.Gly402=
NR_120608.1:n.913C>T
NM_178014.4:c.1206C>T MANE Select NP_821133.1:p.Gly402=
NM_001293212.2:c.1266C>T NP_001280141.1:p.Gly422=
NM_001293213.2:c.600C>T NP_001280142.1:p.Gly200=
NM_001293214.2:c.1074C>T NP_001280143.1:p.Gly358=
NM_001293215.2:c.990C>T NP_001280144.1:p.Gly330=
NM_001293216.2:c.990C>T NP_001280145.1:p.Gly330=
NR_120608.2:n.762C>T