Canonical Allele Identifier: CA448708053
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3155078C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154844C>A , CM000668.2:g.3154844C>A GRCh38
NC_000006.11:g.3155078C>A , CM000668.1:g.3155078C>A GRCh37
NC_000006.10:g.3100077C>A NCBI36
NG_042223.1:g.7706G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.357G>T MANE Select ENSP00000369703.2:p.Val119=
ENST00000679400.1:n.413G>T
ENST00000679907.1:n.745G>T
ENST00000680036.1:n.1139G>T
ENST00000680967.1:n.1447G>T
ENST00000333628.3:c.357G>T ENSP00000369703.2:p.Val119=
ENST00000489942.1:n.552G>T
NM_001069.2:c.357G>T NP_001060.1:p.Val119=
NM_001310315.1:c.102G>T NP_001297244.1:p.Val34=
NM_001069.3:c.357G>T MANE Select NP_001060.1:p.Val119=
NM_001310315.2:c.102G>T NP_001297244.1:p.Val34=