Canonical Allele Identifier: CA497194562

Gene: TUBB3

Linked Data

• MyVariant Identifiers: chr16:g.90002197C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89935789C>T , CM000678.2:g.89935789C>T	GRCh38
NC_000016.9:g.90002197C>T , CM000678.1:g.90002197C>T	GRCh37
NC_000016.8:g.88529698C>T	NCBI36
NG_027810.1:g.18781C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315491.12:c.1338C>T MANE Select	ENSP00000320295.7:p.Ala446=
ENST00000680788.1:n.4759C>T
ENST00000315491.11:c.1338C>T	ENSP00000320295.7:p.Ala446=
ENST00000554444.5:c.1122C>T	ENSP00000451617.1:p.Ala374=
ENST00000555576.5:c.277+2211C>T	ENSP00000452554.1:n.277+2211C>T
ENST00000555609.5:c.*1423C>T	ENSP00000451276.1:n.*1423C>T
ENST00000556922.1:c.2379C>T	ENSP00000451560.1:p.Ala793=
NM_001197181.1:c.1122C>T	NP_001184110.1:p.Ala374=
NM_006086.3:c.1338C>T	NP_006077.2:p.Ala446=
NM_006086.4:c.1338C>T MANE Select	NP_006077.2:p.Ala446=
NM_001197181.2:c.1122C>T	NP_001184110.1:p.Ala374=