Canonical Allele Identifier: CA363141481

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30688331C>G (hg19) ; chr6:g.30720554C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30720554C>G , CM000668.2:g.30720554C>G	GRCh38
NC_000006.11:g.30688331C>G , CM000668.1:g.30688331C>G	GRCh37
NC_000006.10:g.30796310C>G	NCBI36
NG_034142.1:g.5354C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327892.13:c.48C>G MANE Select	ENSP00000339001.7:p.Ile16Met
ENST00000681435.1:c.-159-1983C>G	ENSP00000506665.1:n.-159-1983C>G
ENST00000327892.12:c.48C>G	ENSP00000339001.7:p.Ile16Met
NM_001293213.1:c.48C>G	NP_001280142.1:p.Ile16Met
NM_001293214.1:c.34+14C>G	NP_001280143.1:n.34+14C>G
NM_178014.3:c.48C>G	NP_821133.1:p.Ile16Met
NR_120608.1:n.354C>G
NM_178014.4:c.48C>G MANE Select	NP_821133.1:p.Ile16Met
NM_001293213.2:c.48C>G	NP_001280142.1:p.Ile16Met
NM_001293214.2:c.34+14C>G	NP_001280143.1:n.34+14C>G
NR_120608.2:n.203C>G