Canonical Allele Identifier: CA363141493
Gene: TUBB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.30688332G>A (hg19) chr6:g.30720555G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30720555G>A , CM000668.2:g.30720555G>A GRCh38
NC_000006.11:g.30688332G>A , CM000668.1:g.30688332G>A GRCh37
NC_000006.10:g.30796311G>A NCBI36
NG_034142.1:g.5355G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.49G>A MANE Select ENSP00000339001.7:p.Gly17Ser
ENST00000681435.1:c.-159-1982G>A ENSP00000506665.1:n.-159-1982G>A
ENST00000327892.12:c.49G>A ENSP00000339001.7:p.Gly17Ser
NM_001293213.1:c.49G>A NP_001280142.1:p.Gly17Ser
NM_001293214.1:c.34+15G>A NP_001280143.1:n.34+15G>A
NM_178014.3:c.49G>A NP_821133.1:p.Gly17Ser
NR_120608.1:n.355G>A
NM_178014.4:c.49G>A MANE Select NP_821133.1:p.Gly17Ser
NM_001293213.2:c.49G>A NP_001280142.1:p.Gly17Ser
NM_001293214.2:c.34+15G>A NP_001280143.1:n.34+15G>A
NR_120608.2:n.204G>A
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