Canonical Allele Identifier: CA448707911
Gene: TUBB2A HGNC NCBI

Linked Data

gnomAD v4: 6-3154745-G-T
MyVariant Identifiers: chr6:g.3154979G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154745G>T , CM000668.2:g.3154745G>T GRCh38
NC_000006.11:g.3154979G>T , CM000668.1:g.3154979G>T GRCh37
NC_000006.10:g.3099978G>T NCBI36
NG_042223.1:g.7805C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.456C>A MANE Select ENSP00000369703.2:p.Ile152=
ENST00000679400.1:n.512C>A
ENST00000679907.1:n.844C>A
ENST00000680036.1:n.1238C>A
ENST00000680967.1:n.1546C>A
ENST00000333628.3:c.456C>A ENSP00000369703.2:p.Ile152=
ENST00000489942.1:n.651C>A
NM_001069.2:c.456C>A NP_001060.1:p.Ile152=
NM_001310315.1:c.201C>A NP_001297244.1:p.Ile67=
NM_001069.3:c.456C>A MANE Select NP_001060.1:p.Ile152=
NM_001310315.2:c.201C>A NP_001297244.1:p.Ile67=