Canonical Allele Identifier: CA448707950
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154760G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154526G>A , CM000668.2:g.3154526G>A GRCh38
NC_000006.11:g.3154760G>A , CM000668.1:g.3154760G>A GRCh37
NC_000006.10:g.3099759G>A NCBI36
NG_042223.1:g.8024C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.675C>T MANE Select ENSP00000369703.2:p.Leu225=
ENST00000679400.1:n.731C>T
ENST00000679907.1:n.1063C>T
ENST00000680036.1:n.1457C>T
ENST00000680967.1:n.1765C>T
ENST00000333628.3:c.675C>T ENSP00000369703.2:p.Leu225=
NM_001069.2:c.675C>T NP_001060.1:p.Leu225=
NM_001310315.1:c.420C>T NP_001297244.1:p.Leu140=
NM_001069.3:c.675C>T MANE Select NP_001060.1:p.Leu225=
NM_001310315.2:c.420C>T NP_001297244.1:p.Leu140=