Canonical Allele Identifier: CA362587107
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1389476
ClinVar RCV Id: RCV001897942
dbSNP Id: rs752640088

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225337C>A , CM000668.2:g.3225337C>A GRCh38
NC_000006.11:g.3225571C>A , CM000668.1:g.3225571C>A GRCh37
NC_000006.10:g.3170570C>A NCBI36
NG_016715.1:g.7398G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.752G>T MANE Select ENSP00000259818.6:p.Arg251Leu
ENST00000680070.1:n.1682G>T
ENST00000681707.1:n.1579G>T
ENST00000681757.1:n.1057G>T
ENST00000259818.7:c.752G>T ENSP00000259818.6:p.Arg251Leu
ENST00000473006.1:n.869G>T
NM_178012.4:c.752G>T NP_821080.1:p.Arg251Leu
XM_011514571.1:c.536G>T XP_011512873.1:p.Arg179Leu
NM_178012.5:c.752G>T MANE Select NP_821080.1:p.Arg251Leu