Canonical Allele Identifier: CA8256192

Gene: TUBB3

Linked Data

• dbSNP Id: rs775854497
• ExAC: 16:90001840 C / T
• gnomAD v2: 16-90001840-C-T
• gnomAD v4: 16-89935432-C-T
• COSMIC: COSM1290620
• MyVariant Identifiers: chr16:g.90001840C>T (hg19) ; chr16:g.89935432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89935432C>T , CM000678.2:g.89935432C>T	GRCh38
NC_000016.9:g.90001840C>T , CM000678.1:g.90001840C>T	GRCh37
NC_000016.8:g.88529341C>T	NCBI36
NG_027810.1:g.18424C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000315491.12:c.981C>T MANE Select	ENSP00000320295.7:p.Asp327=
ENST00000680788.1:n.4402C>T
ENST00000315491.11:c.981C>T	ENSP00000320295.7:p.Asp327=
ENST00000554444.5:c.765C>T	ENSP00000451617.1:p.Asp255=
ENST00000555576.5:c.277+1854C>T	ENSP00000452554.1:n.277+1854C>T
ENST00000555609.5:c.*1066C>T	ENSP00000451276.1:n.*1066C>T
ENST00000556922.1:c.2022C>T	ENSP00000451560.1:p.Asp674=
NM_001197181.1:c.765C>T	NP_001184110.1:p.Asp255=
NM_006086.3:c.981C>T	NP_006077.2:p.Asp327=
NM_006086.4:c.981C>T MANE Select	NP_006077.2:p.Asp327=
NM_001197181.2:c.765C>T	NP_001184110.1:p.Asp255=