Canonical Allele Identifier: CA375821562

Gene: TUBB8

Linked Data

• MyVariant Identifiers: chr10:g.94816A>T (hg19) ; chr10:g.48876A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48876A>T , CM000672.2:g.48876A>T	GRCh38
NC_000010.10:g.94816A>T , CM000672.1:g.94816A>T	GRCh37
NC_000010.9:g.84816A>T	NCBI36
NG_046777.1:g.32580T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000568584.6:c.94T>A MANE Select	ENSP00000456206.2:p.Ser32Thr
ENST00000561967.1:c.94T>A	ENSP00000454878.1:p.Ser32Thr
ENST00000562809.1:c.58-151T>A	ENSP00000456899.1:n.58-151T>A
ENST00000563456.1:n.125T>A
ENST00000564130.2:c.18T>A	ENSP00000457610.1:p.Thr6=
ENST00000567466.1:c.18T>A	ENSP00000454914.1:p.Thr6=
ENST00000568584.5:c.94T>A	ENSP00000456206.1:p.Ser32Thr
ENST00000568866.5:c.94T>A	ENSP00000457062.1:p.Ser32Thr
NM_177987.2:c.94T>A	NP_817124.1:p.Ser32Thr
XM_011519458.1:c.-123T>A	XP_011517760.1:n.-123T>A
XM_011519459.1:c.-123T>A	XP_011517761.1:n.-123T>A
XM_011519459.3:c.-123T>A	XP_011517761.1:n.-123T>A
NM_177987.3:c.94T>A MANE Select	NP_817124.1:p.Ser32Thr
NM_001389618.1:c.-123T>A	NP_001376547.1:n.-123T>A
NM_001389619.1:c.-123T>A	NP_001376548.1:n.-123T>A