Canonical Allele Identifier: CA448707900

Gene: TUBB2A

Linked Data

• MyVariant Identifiers: chr6:g.3154967C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3154733C>T , CM000668.2:g.3154733C>T	GRCh38
NC_000006.11:g.3154967C>T , CM000668.1:g.3154967C>T	GRCh37
NC_000006.10:g.3099966C>T	NCBI36
NG_042223.1:g.7817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333628.4:c.468G>A MANE Select	ENSP00000369703.2:p.Arg156=
ENST00000679400.1:n.524G>A
ENST00000679907.1:n.856G>A
ENST00000680036.1:n.1250G>A
ENST00000680967.1:n.1558G>A
ENST00000333628.3:c.468G>A	ENSP00000369703.2:p.Arg156=
ENST00000489942.1:n.663G>A
NM_001069.2:c.468G>A	NP_001060.1:p.Arg156=
NM_001310315.1:c.213G>A	NP_001297244.1:p.Arg71=
NM_001069.3:c.468G>A MANE Select	NP_001060.1:p.Arg156=
NM_001310315.2:c.213G>A	NP_001297244.1:p.Arg71=