Canonical Allele Identifier: CA497194440
Gene: TUBB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.90002083C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935675C>T , CM000678.2:g.89935675C>T GRCh38
NC_000016.9:g.90002083C>T , CM000678.1:g.90002083C>T GRCh37
NC_000016.8:g.88529584C>T NCBI36
NG_027810.1:g.18667C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.1224C>T MANE Select ENSP00000320295.7:p.Phe408=
ENST00000680788.1:n.4645C>T
ENST00000315491.11:c.1224C>T ENSP00000320295.7:p.Phe408=
ENST00000554444.5:c.1008C>T ENSP00000451617.1:p.Phe336=
ENST00000555576.5:c.277+2097C>T ENSP00000452554.1:n.277+2097C>T
ENST00000555609.5:c.*1309C>T ENSP00000451276.1:n.*1309C>T
ENST00000556922.1:c.2265C>T ENSP00000451560.1:p.Phe755=
NM_001197181.1:c.1008C>T NP_001184110.1:p.Phe336=
NM_006086.3:c.1224C>T NP_006077.2:p.Phe408=
NM_006086.4:c.1224C>T MANE Select NP_006077.2:p.Phe408=
NM_001197181.2:c.1008C>T NP_001184110.1:p.Phe336=