Canonical Allele Identifier: CA448707811
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154898C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154664C>G , CM000668.2:g.3154664C>G GRCh38
NC_000006.11:g.3154898C>G , CM000668.1:g.3154898C>G GRCh37
NC_000006.10:g.3099897C>G NCBI36
NG_042223.1:g.7886G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.537G>C MANE Select ENSP00000369703.2:p.Val179=
ENST00000679400.1:n.593G>C
ENST00000679907.1:n.925G>C
ENST00000680036.1:n.1319G>C
ENST00000680967.1:n.1627G>C
ENST00000333628.3:c.537G>C ENSP00000369703.2:p.Val179=
ENST00000489942.1:n.732G>C
NM_001069.2:c.537G>C NP_001060.1:p.Val179=
NM_001310315.1:c.282G>C NP_001297244.1:p.Val94=
NM_001069.3:c.537G>C MANE Select NP_001060.1:p.Val179=
NM_001310315.2:c.282G>C NP_001297244.1:p.Val94=