Canonical Allele Identifier: CA448708081
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154859C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154625C>T , CM000668.2:g.3154625C>T GRCh38
NC_000006.11:g.3154859C>T , CM000668.1:g.3154859C>T GRCh37
NC_000006.10:g.3099858C>T NCBI36
NG_042223.1:g.7925G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.576G>A MANE Select ENSP00000369703.2:p.Leu192=
ENST00000679400.1:n.632G>A
ENST00000679907.1:n.964G>A
ENST00000680036.1:n.1358G>A
ENST00000680967.1:n.1666G>A
ENST00000333628.3:c.576G>A ENSP00000369703.2:p.Leu192=
ENST00000489942.1:n.771G>A
NM_001069.2:c.576G>A NP_001060.1:p.Leu192=
NM_001310315.1:c.321G>A NP_001297244.1:p.Leu107=
NM_001069.3:c.576G>A MANE Select NP_001060.1:p.Leu192=
NM_001310315.2:c.321G>A NP_001297244.1:p.Leu107=