Canonical Allele Identifier: CA448707476
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225594C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225360C>A , CM000668.2:g.3225360C>A GRCh38
NC_000006.11:g.3225594C>A , CM000668.1:g.3225594C>A GRCh37
NC_000006.10:g.3170593C>A NCBI36
NG_016715.1:g.7375G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.729G>T MANE Select ENSP00000259818.6:p.Pro243=
ENST00000680070.1:n.1659G>T
ENST00000681707.1:n.1556G>T
ENST00000681757.1:n.1034G>T
ENST00000259818.7:c.729G>T ENSP00000259818.6:p.Pro243=
ENST00000473006.1:n.846G>T
NM_178012.4:c.729G>T NP_821080.1:p.Pro243=
XM_011514571.1:c.513G>T XP_011512873.1:p.Pro171=
NM_178012.5:c.729G>T MANE Select NP_821080.1:p.Pro243=