Canonical Allele Identifier: CA448708145
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225837G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225603G>T , CM000668.2:g.3225603G>T GRCh38
NC_000006.11:g.3225837G>T , CM000668.1:g.3225837G>T GRCh37
NC_000006.10:g.3170836G>T NCBI36
NG_016715.1:g.7132C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.486C>A MANE Select ENSP00000259818.6:p.Arg162=
ENST00000680070.1:n.1416C>A
ENST00000681707.1:n.1313C>A
ENST00000681757.1:n.791C>A
ENST00000259818.7:c.486C>A ENSP00000259818.6:p.Arg162=
ENST00000473006.1:n.603C>A
NM_178012.4:c.486C>A NP_821080.1:p.Arg162=
XM_011514571.1:c.270C>A XP_011512873.1:p.Arg90=
NM_178012.5:c.486C>A MANE Select NP_821080.1:p.Arg162=