Canonical Allele Identifier: CA497381380
Gene: TUBB3 HGNC NCBI

Linked Data

dbSNP Id: rs201682024
MyVariant Identifiers: chr16:g.90001714C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935306C>A , CM000678.2:g.89935306C>A GRCh38
NC_000016.9:g.90001714C>A , CM000678.1:g.90001714C>A GRCh37
NC_000016.8:g.88529215C>A NCBI36
NG_027810.1:g.18298C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.855C>A MANE Select ENSP00000320295.7:p.Thr285=
ENST00000680788.1:n.4276C>A
ENST00000315491.11:c.855C>A ENSP00000320295.7:p.Thr285=
ENST00000554444.5:c.639C>A ENSP00000451617.1:p.Thr213=
ENST00000555576.5:c.277+1728C>A ENSP00000452554.1:n.277+1728C>A
ENST00000555609.5:c.*940C>A ENSP00000451276.1:n.*940C>A
ENST00000556922.1:c.1896C>A ENSP00000451560.1:p.Thr632=
NM_001197181.1:c.639C>A NP_001184110.1:p.Thr213=
NM_006086.3:c.855C>A NP_006077.2:p.Thr285=
NM_006086.4:c.855C>A MANE Select NP_006077.2:p.Thr285=
NM_001197181.2:c.639C>A NP_001184110.1:p.Thr213=