Canonical Allele Identifier: CA448707834
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154673C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154439C>G , CM000668.2:g.3154439C>G GRCh38
NC_000006.11:g.3154673C>G , CM000668.1:g.3154673C>G GRCh37
NC_000006.10:g.3099672C>G NCBI36
NG_042223.1:g.8111G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.762G>C MANE Select ENSP00000369703.2:p.Ala254=
ENST00000679400.1:n.818G>C
ENST00000679907.1:n.1150G>C
ENST00000680036.1:n.1544G>C
ENST00000680967.1:n.1852G>C
ENST00000333628.3:c.762G>C ENSP00000369703.2:p.Ala254=
NM_001069.2:c.762G>C NP_001060.1:p.Ala254=
NM_001310315.1:c.507G>C NP_001297244.1:p.Ala169=
NM_001069.3:c.762G>C MANE Select NP_001060.1:p.Ala254=
NM_001310315.2:c.507G>C NP_001297244.1:p.Ala169=