Canonical Allele Identifier: CA448708170
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs111690866
MyVariant Identifiers: chr6:g.3225876G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225642G>A , CM000668.2:g.3225642G>A GRCh38
NC_000006.11:g.3225876G>A , CM000668.1:g.3225876G>A GRCh37
NC_000006.10:g.3170875G>A NCBI36
NG_016715.1:g.7093C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.447C>T MANE Select ENSP00000259818.6:p.Thr149=
ENST00000680070.1:n.1377C>T
ENST00000681707.1:n.1274C>T
ENST00000681757.1:n.752C>T
ENST00000259818.7:c.447C>T ENSP00000259818.6:p.Thr149=
ENST00000473006.1:n.564C>T
NM_178012.4:c.447C>T NP_821080.1:p.Thr149=
XM_011514571.1:c.231C>T XP_011512873.1:p.Thr77=
NM_178012.5:c.447C>T MANE Select NP_821080.1:p.Thr149=
Search 100 bp 5'
Search 100 bp 3'