Canonical Allele Identifier: CA251179
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 160181
ClinVar RCV Id: RCV000147837 RCV003764894
dbSNP Id: rs587784499
ExAC: 6:3225825 G / A
gnomAD v2: 6-3225825-G-A
gnomAD v3: 6-3225591-G-A
gnomAD v4: 6-3225591-G-A
MyVariant Identifiers: chr6:g.3225825G>A (hg19) chr6:g.3225591G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225591G>A , CM000668.2:g.3225591G>A GRCh38
NC_000006.11:g.3225825G>A , CM000668.1:g.3225825G>A GRCh37
NC_000006.10:g.3170824G>A NCBI36
NG_016715.1:g.7144C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.498C>T MANE Select ENSP00000259818.6:p.Thr166=
ENST00000680070.1:n.1428C>T
ENST00000681707.1:n.1325C>T
ENST00000681757.1:n.803C>T
ENST00000259818.7:c.498C>T ENSP00000259818.6:p.Thr166=
ENST00000473006.1:n.615C>T
NM_178012.4:c.498C>T NP_821080.1:p.Thr166=
XM_011514571.1:c.282C>T XP_011512873.1:p.Thr94=
NM_178012.5:c.498C>T MANE Select NP_821080.1:p.Thr166=
Search 100 bp 5'
Search 100 bp 3'