Canonical Allele Identifier: CA448707844
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154922G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154688G>C , CM000668.2:g.3154688G>C GRCh38
NC_000006.11:g.3154922G>C , CM000668.1:g.3154922G>C GRCh37
NC_000006.10:g.3099921G>C NCBI36
NG_042223.1:g.7862C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.513C>G MANE Select ENSP00000369703.2:p.Pro171=
ENST00000679400.1:n.569C>G
ENST00000679907.1:n.901C>G
ENST00000680036.1:n.1295C>G
ENST00000680967.1:n.1603C>G
ENST00000333628.3:c.513C>G ENSP00000369703.2:p.Pro171=
ENST00000489942.1:n.708C>G
NM_001069.2:c.513C>G NP_001060.1:p.Pro171=
NM_001310315.1:c.258C>G NP_001297244.1:p.Pro86=
NM_001069.3:c.513C>G MANE Select NP_001060.1:p.Pro171=
NM_001310315.2:c.258C>G NP_001297244.1:p.Pro86=