Canonical Allele Identifier: CA448708252
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225987C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225753C>T , CM000668.2:g.3225753C>T GRCh38
NC_000006.11:g.3225987C>T , CM000668.1:g.3225987C>T GRCh37
NC_000006.10:g.3170986C>T NCBI36
NG_016715.1:g.6982G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.336G>A MANE Select ENSP00000259818.6:p.Leu112=
ENST00000680070.1:n.1266G>A
ENST00000681707.1:n.1163G>A
ENST00000681757.1:n.641G>A
ENST00000259818.7:c.336G>A ENSP00000259818.6:p.Leu112=
ENST00000473006.1:n.453G>A
NM_178012.4:c.336G>A NP_821080.1:p.Leu112=
XM_011514571.1:c.120G>A XP_011512873.1:p.Leu40=
NM_178012.5:c.336G>A MANE Select NP_821080.1:p.Leu112=