Canonical Allele Identifier: CA362586631
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 437125
ClinVar RCV Id: RCV000503116 RCV001291305
dbSNP Id: rs1554126886
MyVariant Identifiers: chr6:g.3225452G>T (hg19) chr6:g.3225218G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225218G>T , CM000668.2:g.3225218G>T GRCh38
NC_000006.11:g.3225452G>T , CM000668.1:g.3225452G>T GRCh37
NC_000006.10:g.3170451G>T NCBI36
NG_016715.1:g.7517C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.871C>A MANE Select ENSP00000259818.6:p.Gln291Lys
ENST00000680070.1:n.1801C>A
ENST00000681707.1:n.1698C>A
ENST00000681757.1:n.1176C>A
ENST00000259818.7:c.871C>A ENSP00000259818.6:p.Gln291Lys
ENST00000473006.1:n.988C>A
NM_178012.4:c.871C>A NP_821080.1:p.Gln291Lys
XM_011514571.1:c.655C>A XP_011512873.1:p.Gln219Lys
NM_178012.5:c.871C>A MANE Select NP_821080.1:p.Gln291Lys
Search 100 bp 5'
Search 100 bp 3'