Canonical Allele Identifier: CA375821222

Gene: TUBB8

Linked Data

• gnomAD v4: 10-48779-G-T
• MyVariant Identifiers: chr10:g.94719G>T (hg19) ; chr10:g.48779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48779G>T , CM000672.2:g.48779G>T	GRCh38
NC_000010.10:g.94719G>T , CM000672.1:g.94719G>T	GRCh37
NC_000010.9:g.84719G>T	NCBI36
NG_046777.1:g.32677C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000568584.6:c.166+25C>A MANE Select	ENSP00000456206.2:n.166+25C>A
ENST00000561967.1:c.166+25C>A	ENSP00000454878.1:n.166+25C>A
ENST00000562809.1:c.58-54C>A	ENSP00000456899.1:n.58-54C>A
ENST00000563456.1:n.222C>A
ENST00000564130.2:c.115C>A	ENSP00000457610.1:p.Arg39Ser
ENST00000567466.1:c.90+25C>A	ENSP00000454914.1:n.90+25C>A
ENST00000568584.5:c.166+25C>A	ENSP00000456206.1:n.166+25C>A
ENST00000568866.5:c.166+25C>A	ENSP00000457062.1:n.166+25C>A
NM_177987.2:c.166+25C>A	NP_817124.1:n.166+25C>A
XM_011519458.1:c.-51+25C>A	XP_011517760.1:n.-51+25C>A
XM_011519459.1:c.-51+25C>A	XP_011517761.1:n.-51+25C>A
XM_011519459.3:c.-51+25C>A	XP_011517761.1:n.-51+25C>A
NM_177987.3:c.166+25C>A MANE Select	NP_817124.1:n.166+25C>A
NM_001389618.1:c.-51+25C>A	NP_001376547.1:n.-51+25C>A
NM_001389619.1:c.-51+25C>A	NP_001376548.1:n.-51+25C>A