Canonical Allele Identifier: CA448708029
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154817G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154583G>T , CM000668.2:g.3154583G>T GRCh38
NC_000006.11:g.3154817G>T , CM000668.1:g.3154817G>T GRCh37
NC_000006.10:g.3099816G>T NCBI36
NG_042223.1:g.7967C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.618C>A MANE Select ENSP00000369703.2:p.Ala206=
ENST00000679400.1:n.674C>A
ENST00000679907.1:n.1006C>A
ENST00000680036.1:n.1400C>A
ENST00000680967.1:n.1708C>A
ENST00000333628.3:c.618C>A ENSP00000369703.2:p.Ala206=
ENST00000489942.1:n.813C>A
NM_001069.2:c.618C>A NP_001060.1:p.Ala206=
NM_001310315.1:c.363C>A NP_001297244.1:p.Ala121=
NM_001069.3:c.618C>A MANE Select NP_001060.1:p.Ala206=
NM_001310315.2:c.363C>A NP_001297244.1:p.Ala121=