Canonical Allele Identifier: CA375821567

Gene: TUBB8

Linked Data

• gnomAD v4: 10-48878-T-C
• MyVariant Identifiers: chr10:g.94818T>C (hg19) ; chr10:g.48878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48878T>C , CM000672.2:g.48878T>C	GRCh38
NC_000010.10:g.94818T>C , CM000672.1:g.94818T>C	GRCh37
NC_000010.9:g.84818T>C	NCBI36
NG_046777.1:g.32578A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000568584.6:c.92A>G MANE Select	ENSP00000456206.2:p.Asp31Gly
ENST00000561967.1:c.92A>G	ENSP00000454878.1:p.Asp31Gly
ENST00000562809.1:c.58-153A>G	ENSP00000456899.1:n.58-153A>G
ENST00000563456.1:n.123A>G
ENST00000564130.2:c.16A>G	ENSP00000457610.1:p.Thr6Ala
ENST00000567466.1:c.16A>G	ENSP00000454914.1:p.Thr6Ala
ENST00000568584.5:c.92A>G	ENSP00000456206.1:p.Asp31Gly
ENST00000568866.5:c.92A>G	ENSP00000457062.1:p.Asp31Gly
NM_177987.2:c.92A>G	NP_817124.1:p.Asp31Gly
XM_011519458.1:c.-125A>G	XP_011517760.1:n.-125A>G
XM_011519459.1:c.-125A>G	XP_011517761.1:n.-125A>G
XM_011519459.3:c.-125A>G	XP_011517761.1:n.-125A>G
NM_177987.3:c.92A>G MANE Select	NP_817124.1:p.Asp31Gly
NM_001389618.1:c.-125A>G	NP_001376547.1:n.-125A>G
NM_001389619.1:c.-125A>G	NP_001376548.1:n.-125A>G