Canonical Allele Identifier: CA624455591

Gene: TUBB3

Linked Data

• dbSNP Id: rs1270952495
• gnomAD v2: 16-90002231-T-C
• gnomAD v4: 16-89935823-T-C
• MyVariant Identifiers: chr16:g.90002231T>C (hg19) ; chr16:g.89935823T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89935823T>C , CM000678.2:g.89935823T>C	GRCh38
NC_000016.9:g.90002231T>C , CM000678.1:g.90002231T>C	GRCh37
NC_000016.8:g.88529732T>C	NCBI36
NG_027810.1:g.18815T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315491.12:c.*19T>C MANE Select	ENSP00000320295.7:n.*19T>C
ENST00000680788.1:n.4793T>C
ENST00000315491.11:c.*19T>C	ENSP00000320295.7:n.*19T>C
ENST00000554444.5:c.*19T>C	ENSP00000451617.1:n.*19T>C
ENST00000555576.5:c.277+2245T>C	ENSP00000452554.1:n.277+2245T>C
ENST00000555609.5:c.*1457T>C	ENSP00000451276.1:n.*1457T>C
ENST00000556922.1:c.*19T>C	ENSP00000451560.1:n.*19T>C
NM_001197181.1:c.*19T>C	NP_001184110.1:n.*19T>C
NM_006086.3:c.*19T>C	NP_006077.2:n.*19T>C
NM_006086.4:c.*19T>C MANE Select	NP_006077.2:n.*19T>C
NM_001197181.2:c.*19T>C	NP_001184110.1:n.*19T>C