Canonical Allele Identifier: CA448707878
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154949G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154715G>T , CM000668.2:g.3154715G>T GRCh38
NC_000006.11:g.3154949G>T , CM000668.1:g.3154949G>T GRCh37
NC_000006.10:g.3099948G>T NCBI36
NG_042223.1:g.7835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.486C>A MANE Select ENSP00000369703.2:p.Arg162=
ENST00000679400.1:n.542C>A
ENST00000679907.1:n.874C>A
ENST00000680036.1:n.1268C>A
ENST00000680967.1:n.1576C>A
ENST00000333628.3:c.486C>A ENSP00000369703.2:p.Arg162=
ENST00000489942.1:n.681C>A
NM_001069.2:c.486C>A NP_001060.1:p.Arg162=
NM_001310315.1:c.231C>A NP_001297244.1:p.Arg77=
NM_001069.3:c.486C>A MANE Select NP_001060.1:p.Arg162=
NM_001310315.2:c.231C>A NP_001297244.1:p.Arg77=