Canonical Allele Identifier: CA448707483
Gene: TUBB2B HGNC NCBI

Linked Data

gnomAD v4: 6-3225363-G-A
MyVariant Identifiers: chr6:g.3225597G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225363G>A , CM000668.2:g.3225363G>A GRCh38
NC_000006.11:g.3225597G>A , CM000668.1:g.3225597G>A GRCh37
NC_000006.10:g.3170596G>A NCBI36
NG_016715.1:g.7372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.726C>T MANE Select ENSP00000259818.6:p.Phe242=
ENST00000680070.1:n.1656C>T
ENST00000681707.1:n.1553C>T
ENST00000681757.1:n.1031C>T
ENST00000259818.7:c.726C>T ENSP00000259818.6:p.Phe242=
ENST00000473006.1:n.843C>T
NM_178012.4:c.726C>T NP_821080.1:p.Phe242=
XM_011514571.1:c.510C>T XP_011512873.1:p.Phe170=
NM_178012.5:c.726C>T MANE Select NP_821080.1:p.Phe242=