Canonical Allele Identifier: CA448707487
Gene: TUBB2B HGNC NCBI

Linked Data

gnomAD v4: 6-3225201-G-T
MyVariant Identifiers: chr6:g.3225435G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225201G>T , CM000668.2:g.3225201G>T GRCh38
NC_000006.11:g.3225435G>T , CM000668.1:g.3225435G>T GRCh37
NC_000006.10:g.3170434G>T NCBI36
NG_016715.1:g.7534C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.888C>A MANE Select ENSP00000259818.6:p.Ser296=
ENST00000680070.1:n.1818C>A
ENST00000681707.1:n.1715C>A
ENST00000681757.1:n.1193C>A
ENST00000259818.7:c.888C>A ENSP00000259818.6:p.Ser296=
ENST00000473006.1:n.1005C>A
NM_178012.4:c.888C>A NP_821080.1:p.Ser296=
XM_011514571.1:c.672C>A XP_011512873.1:p.Ser224=
NM_178012.5:c.888C>A MANE Select NP_821080.1:p.Ser296=