Canonical Allele Identifier: CA397477135
Gene: TUBB3 HGNC NCBI

Linked Data

dbSNP Id: rs2151093136

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935728A>C , CM000678.2:g.89935728A>C GRCh38
NC_000016.9:g.90002136A>C , CM000678.1:g.90002136A>C GRCh37
NC_000016.8:g.88529637A>C NCBI36
NG_027810.1:g.18720A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.1277A>C MANE Select ENSP00000320295.7:p.Gln426Pro
ENST00000680788.1:n.4698A>C
ENST00000315491.11:c.1277A>C ENSP00000320295.7:p.Gln426Pro
ENST00000554444.5:c.1061A>C ENSP00000451617.1:p.Gln354Pro
ENST00000555576.5:c.277+2150A>C ENSP00000452554.1:n.277+2150A>C
ENST00000555609.5:c.*1362A>C ENSP00000451276.1:n.*1362A>C
ENST00000556922.1:c.2318A>C ENSP00000451560.1:p.Gln773Pro
NM_001197181.1:c.1061A>C NP_001184110.1:p.Gln354Pro
NM_006086.3:c.1277A>C NP_006077.2:p.Gln426Pro
NM_006086.4:c.1277A>C MANE Select NP_006077.2:p.Gln426Pro
NM_001197181.2:c.1061A>C NP_001184110.1:p.Gln354Pro