Canonical Allele Identifier: CA980479332
Gene: TUBB3 HGNC NCBI

Linked Data

dbSNP Id: rs2030442850

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935918T>A , CM000678.2:g.89935918T>A GRCh38
NC_000016.9:g.90002326T>A , CM000678.1:g.90002326T>A GRCh37
NC_000016.8:g.88529827T>A NCBI36
NG_027810.1:g.18910T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.*114T>A MANE Select ENSP00000320295.7:n.*114T>A
ENST00000680788.1:n.4888T>A
ENST00000315491.11:c.*114T>A ENSP00000320295.7:n.*114T>A
ENST00000554444.5:c.*114T>A ENSP00000451617.1:n.*114T>A
ENST00000555576.5:c.277+2340T>A ENSP00000452554.1:n.277+2340T>A
ENST00000555609.5:c.*1552T>A ENSP00000451276.1:n.*1552T>A
ENST00000556922.1:c.*114T>A ENSP00000451560.1:n.*114T>A
NM_001197181.1:c.*114T>A NP_001184110.1:n.*114T>A
NM_006086.3:c.*114T>A NP_006077.2:n.*114T>A
NM_006086.4:c.*114T>A MANE Select NP_006077.2:n.*114T>A
NM_001197181.2:c.*114T>A NP_001184110.1:n.*114T>A