Canonical Allele Identifier: CA448707879
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154952G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154718G>A , CM000668.2:g.3154718G>A GRCh38
NC_000006.11:g.3154952G>A , CM000668.1:g.3154952G>A GRCh37
NC_000006.10:g.3099951G>A NCBI36
NG_042223.1:g.7832C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.483C>T MANE Select ENSP00000369703.2:p.Asp161=
ENST00000679400.1:n.539C>T
ENST00000679907.1:n.871C>T
ENST00000680036.1:n.1265C>T
ENST00000680967.1:n.1573C>T
ENST00000333628.3:c.483C>T ENSP00000369703.2:p.Asp161=
ENST00000489942.1:n.678C>T
NM_001069.2:c.483C>T NP_001060.1:p.Asp161=
NM_001310315.1:c.228C>T NP_001297244.1:p.Asp76=
NM_001069.3:c.483C>T MANE Select NP_001060.1:p.Asp161=
NM_001310315.2:c.228C>T NP_001297244.1:p.Asp76=