Canonical Allele Identifier: CA448707619
Gene: TUBB2B HGNC NCBI

Linked Data

gnomAD v4: 6-3225432-G-A
MyVariant Identifiers: chr6:g.3225666G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225432G>A , CM000668.2:g.3225432G>A GRCh38
NC_000006.11:g.3225666G>A , CM000668.1:g.3225666G>A GRCh37
NC_000006.10:g.3170665G>A NCBI36
NG_016715.1:g.7303C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.657C>T MANE Select ENSP00000259818.6:p.Thr219=
ENST00000680070.1:n.1587C>T
ENST00000681707.1:n.1484C>T
ENST00000681757.1:n.962C>T
ENST00000259818.7:c.657C>T ENSP00000259818.6:p.Thr219=
ENST00000473006.1:n.774C>T
NM_178012.4:c.657C>T NP_821080.1:p.Thr219=
XM_011514571.1:c.441C>T XP_011512873.1:p.Thr147=
NM_178012.5:c.657C>T MANE Select NP_821080.1:p.Thr219=