Canonical Allele Identifier: CA362592355
Gene: TUBB2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3236669
ClinVar RCV Id: RCV004556129

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154592A>C , CM000668.2:g.3154592A>C GRCh38
NC_000006.11:g.3154826A>C , CM000668.1:g.3154826A>C GRCh37
NC_000006.10:g.3099825A>C NCBI36
NG_042223.1:g.7958T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.609T>G MANE Select ENSP00000369703.2:p.Asp203Glu
ENST00000679400.1:n.665T>G
ENST00000679907.1:n.997T>G
ENST00000680036.1:n.1391T>G
ENST00000680967.1:n.1699T>G
ENST00000333628.3:c.609T>G ENSP00000369703.2:p.Asp203Glu
ENST00000489942.1:n.804T>G
NM_001069.2:c.609T>G NP_001060.1:p.Asp203Glu
NM_001310315.1:c.354T>G NP_001297244.1:p.Asp118Glu
NM_001069.3:c.609T>G MANE Select NP_001060.1:p.Asp203Glu
NM_001310315.2:c.354T>G NP_001297244.1:p.Asp118Glu