Canonical Allele Identifier: CA136809689

Gene: TUBB

Linked Data

• dbSNP Id: rs3873306
• MyVariant Identifiers: chr6:g.30692082A>G (hg19) ; chr6:g.30724305A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724305A>G , CM000668.2:g.30724305A>G	GRCh38
NC_000006.11:g.30692082A>G , CM000668.1:g.30692082A>G	GRCh37
NC_000006.10:g.30800061A>G	NCBI36
NG_034142.1:g.9105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1243A>G MANE Select	ENSP00000339001.7:p.Met415Val
ENST00000680530.1:n.2105A>G
ENST00000681421.1:n.2309A>G
ENST00000681435.1:c.1027A>G	ENSP00000506665.1:p.Met343Val
ENST00000327892.12:c.1243A>G	ENSP00000339001.7:p.Met415Val
ENST00000330914.7:c.1027A>G	ENSP00000365578.2:p.Met343Val
ENST00000396384.1:c.1027A>G	ENSP00000379668.1:p.Met343Val
ENST00000396389.5:c.1189A>G	ENSP00000379672.1:p.Met397Val
NM_001293212.1:c.1303A>G	NP_001280141.1:p.Met435Val
NM_001293213.1:c.637A>G	NP_001280142.1:p.Met213Val
NM_001293214.1:c.1111A>G	NP_001280143.1:p.Met371Val
NM_001293215.1:c.1027A>G	NP_001280144.1:p.Met343Val
NM_001293216.1:c.1027A>G	NP_001280145.1:p.Met343Val
NM_178014.3:c.1243A>G	NP_821133.1:p.Met415Val
NR_120608.1:n.950A>G
NM_178014.4:c.1243A>G MANE Select	NP_821133.1:p.Met415Val
NM_001293212.2:c.1303A>G	NP_001280141.1:p.Met435Val
NM_001293213.2:c.637A>G	NP_001280142.1:p.Met213Val
NM_001293214.2:c.1111A>G	NP_001280143.1:p.Met371Val
NM_001293215.2:c.1027A>G	NP_001280144.1:p.Met343Val
NM_001293216.2:c.1027A>G	NP_001280145.1:p.Met343Val
NR_120608.2:n.799A>G