Canonical Allele Identifier: CA448707886
Gene: TUBB2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3154715C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154481C>T , CM000668.2:g.3154481C>T GRCh38
NC_000006.11:g.3154715C>T , CM000668.1:g.3154715C>T GRCh37
NC_000006.10:g.3099714C>T NCBI36
NG_042223.1:g.8069G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333628.4:c.720G>A MANE Select ENSP00000369703.2:p.Leu240=
ENST00000679400.1:n.776G>A
ENST00000679907.1:n.1108G>A
ENST00000680036.1:n.1502G>A
ENST00000680967.1:n.1810G>A
ENST00000333628.3:c.720G>A ENSP00000369703.2:p.Leu240=
NM_001069.2:c.720G>A NP_001060.1:p.Leu240=
NM_001310315.1:c.465G>A NP_001297244.1:p.Leu155=
NM_001069.3:c.720G>A MANE Select NP_001060.1:p.Leu240=
NM_001310315.2:c.465G>A NP_001297244.1:p.Leu155=
Search 100 bp 5'
Search 100 bp 3'