Canonical Allele Identifier: CA250426
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 428
ClinVar RCV Id: RCV000000456
dbSNP Id: rs137853196

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225296A>G , CM000668.2:g.3225296A>G GRCh38
NC_000006.11:g.3225530A>G , CM000668.1:g.3225530A>G GRCh37
NC_000006.10:g.3170529A>G NCBI36
NG_016715.1:g.7439T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.793T>C MANE Select ENSP00000259818.6:p.Phe265Leu
ENST00000680070.1:n.1723T>C
ENST00000681707.1:n.1620T>C
ENST00000681757.1:n.1098T>C
ENST00000259818.7:c.793T>C ENSP00000259818.6:p.Phe265Leu
ENST00000473006.1:n.910T>C
NM_178012.4:c.793T>C NP_821080.1:p.Phe265Leu
XM_011514571.1:c.577T>C XP_011512873.1:p.Phe193Leu
NM_178012.5:c.793T>C MANE Select NP_821080.1:p.Phe265Leu