Canonical Allele Identifier: CA448707780
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154874G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154640G>T , CM000668.2:g.3154640G>T GRCh38
NC_000006.11:g.3154874G>T , CM000668.1:g.3154874G>T GRCh37
NC_000006.10:g.3099873G>T NCBI36
NG_042223.1:g.7910C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.561C>A MANE Select ENSP00000369703.2:p.Leu187=
ENST00000679400.1:n.617C>A
ENST00000679907.1:n.949C>A
ENST00000680036.1:n.1343C>A
ENST00000680967.1:n.1651C>A
ENST00000333628.3:c.561C>A ENSP00000369703.2:p.Leu187=
ENST00000489942.1:n.756C>A
NM_001069.2:c.561C>A NP_001060.1:p.Leu187=
NM_001310315.1:c.306C>A NP_001297244.1:p.Leu102=
NM_001069.3:c.561C>A MANE Select NP_001060.1:p.Leu187=
NM_001310315.2:c.306C>A NP_001297244.1:p.Leu102=