Canonical Allele Identifier: CA448707357
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225537G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225303G>T , CM000668.2:g.3225303G>T GRCh38
NC_000006.11:g.3225537G>T , CM000668.1:g.3225537G>T GRCh37
NC_000006.10:g.3170536G>T NCBI36
NG_016715.1:g.7432C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.786C>A MANE Select ENSP00000259818.6:p.Arg262=
ENST00000680070.1:n.1716C>A
ENST00000681707.1:n.1613C>A
ENST00000681757.1:n.1091C>A
ENST00000259818.7:c.786C>A ENSP00000259818.6:p.Arg262=
ENST00000473006.1:n.903C>A
NM_178012.4:c.786C>A NP_821080.1:p.Arg262=
XM_011514571.1:c.570C>A XP_011512873.1:p.Arg190=
NM_178012.5:c.786C>A MANE Select NP_821080.1:p.Arg262=