Canonical Allele Identifier: CA251185
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 160186
ClinVar RCV Id: RCV000147844
dbSNP Id: rs587784501
MyVariant Identifiers: chr6:g.3225464G>A (hg19) chr6:g.3225230G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225230G>A , CM000668.2:g.3225230G>A GRCh38
NC_000006.11:g.3225464G>A , CM000668.1:g.3225464G>A GRCh37
NC_000006.10:g.3170463G>A NCBI36
NG_016715.1:g.7505C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.859C>T MANE Select ENSP00000259818.6:p.Pro287Ser
ENST00000680070.1:n.1789C>T
ENST00000681707.1:n.1686C>T
ENST00000681757.1:n.1164C>T
ENST00000259818.7:c.859C>T ENSP00000259818.6:p.Pro287Ser
ENST00000473006.1:n.976C>T
NM_178012.4:c.859C>T NP_821080.1:p.Pro287Ser
XM_011514571.1:c.643C>T XP_011512873.1:p.Pro215Ser
NM_178012.5:c.859C>T MANE Select NP_821080.1:p.Pro287Ser
Search 100 bp 5'
Search 100 bp 3'