Canonical Allele Identifier: CA448707794
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154889G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154655G>A , CM000668.2:g.3154655G>A GRCh38
NC_000006.11:g.3154889G>A , CM000668.1:g.3154889G>A GRCh37
NC_000006.10:g.3099888G>A NCBI36
NG_042223.1:g.7895C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.546C>T MANE Select ENSP00000369703.2:p.Pro182=
ENST00000679400.1:n.602C>T
ENST00000679907.1:n.934C>T
ENST00000680036.1:n.1328C>T
ENST00000680967.1:n.1636C>T
ENST00000333628.3:c.546C>T ENSP00000369703.2:p.Pro182=
ENST00000489942.1:n.741C>T
NM_001069.2:c.546C>T NP_001060.1:p.Pro182=
NM_001310315.1:c.291C>T NP_001297244.1:p.Pro97=
NM_001069.3:c.546C>T MANE Select NP_001060.1:p.Pro182=
NM_001310315.2:c.291C>T NP_001297244.1:p.Pro97=