Canonical Allele Identifier: CA448707837
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154919T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154685T>A , CM000668.2:g.3154685T>A GRCh38
NC_000006.11:g.3154919T>A , CM000668.1:g.3154919T>A GRCh37
NC_000006.10:g.3099918T>A NCBI36
NG_042223.1:g.7865A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.516A>T MANE Select ENSP00000369703.2:p.Ser172=
ENST00000679400.1:n.572A>T
ENST00000679907.1:n.904A>T
ENST00000680036.1:n.1298A>T
ENST00000680967.1:n.1606A>T
ENST00000333628.3:c.516A>T ENSP00000369703.2:p.Ser172=
ENST00000489942.1:n.711A>T
NM_001069.2:c.516A>T NP_001060.1:p.Ser172=
NM_001310315.1:c.261A>T NP_001297244.1:p.Ser87=
NM_001069.3:c.516A>T MANE Select NP_001060.1:p.Ser172=
NM_001310315.2:c.261A>T NP_001297244.1:p.Ser87=