Canonical Allele Identifier: CA362589434
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 996659
ClinVar RCV Id: RCV001291307
dbSNP Id: rs1757279879
MyVariant Identifiers: chr6:g.3226025T>A (hg19) chr6:g.3225791T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225791T>A , CM000668.2:g.3225791T>A GRCh38
NC_000006.11:g.3226025T>A , CM000668.1:g.3226025T>A GRCh37
NC_000006.10:g.3171024T>A NCBI36
NG_016715.1:g.6944A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.298A>T MANE Select ENSP00000259818.6:p.Asn100Tyr
ENST00000680070.1:n.1228A>T
ENST00000681707.1:n.1125A>T
ENST00000681757.1:n.603A>T
ENST00000259818.7:c.298A>T ENSP00000259818.6:p.Asn100Tyr
ENST00000473006.1:n.415A>T
NM_178012.4:c.298A>T NP_821080.1:p.Asn100Tyr
XM_011514571.1:c.82A>T XP_011512873.1:p.Asn28Tyr
NM_178012.5:c.298A>T MANE Select NP_821080.1:p.Asn100Tyr
Search 100 bp 5'
Search 100 bp 3'