Canonical Allele Identifier: CA362586715
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 3235893
ClinVar RCV Id: RCV004555154

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225244C>G , CM000668.2:g.3225244C>G GRCh38
NC_000006.11:g.3225478C>G , CM000668.1:g.3225478C>G GRCh37
NC_000006.10:g.3170477C>G NCBI36
NG_016715.1:g.7491G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.845G>C MANE Select ENSP00000259818.6:p.Arg282Pro
ENST00000680070.1:n.1775G>C
ENST00000681707.1:n.1672G>C
ENST00000681757.1:n.1150G>C
ENST00000259818.7:c.845G>C ENSP00000259818.6:p.Arg282Pro
ENST00000473006.1:n.962G>C
NM_178012.4:c.845G>C NP_821080.1:p.Arg282Pro
XM_011514571.1:c.629G>C XP_011512873.1:p.Arg210Pro
NM_178012.5:c.845G>C MANE Select NP_821080.1:p.Arg282Pro