Canonical Allele Identifier: CA448707823

Gene: TUBB2A

Linked Data

• ClinVar Variation Id: 2182506
• ClinVar RCV Id: RCV002592047
• MyVariant Identifiers: chr6:g.3154907T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3154673T>G , CM000668.2:g.3154673T>G	GRCh38
NC_000006.11:g.3154907T>G , CM000668.1:g.3154907T>G	GRCh37
NC_000006.10:g.3099906T>G	NCBI36
NG_042223.1:g.7877A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333628.4:c.528A>C MANE Select	ENSP00000369703.2:p.Ser176=
ENST00000679400.1:n.584A>C
ENST00000679907.1:n.916A>C
ENST00000680036.1:n.1310A>C
ENST00000680967.1:n.1618A>C
ENST00000333628.3:c.528A>C	ENSP00000369703.2:p.Ser176=
ENST00000489942.1:n.723A>C
NM_001069.2:c.528A>C	NP_001060.1:p.Ser176=
NM_001310315.1:c.273A>C	NP_001297244.1:p.Ser91=
NM_001069.3:c.528A>C MANE Select	NP_001060.1:p.Ser176=
NM_001310315.2:c.273A>C	NP_001297244.1:p.Ser91=