Canonical Allele Identifier: CA497194435
Gene: TUBB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.90002059C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935651C>G , CM000678.2:g.89935651C>G GRCh38
NC_000016.9:g.90002059C>G , CM000678.1:g.90002059C>G GRCh37
NC_000016.8:g.88529560C>G NCBI36
NG_027810.1:g.18643C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.1200C>G MANE Select ENSP00000320295.7:p.Gly400=
ENST00000680788.1:n.4621C>G
ENST00000315491.11:c.1200C>G ENSP00000320295.7:p.Gly400=
ENST00000554444.5:c.984C>G ENSP00000451617.1:p.Gly328=
ENST00000555576.5:c.277+2073C>G ENSP00000452554.1:n.277+2073C>G
ENST00000555609.5:c.*1285C>G ENSP00000451276.1:n.*1285C>G
ENST00000556922.1:c.2241C>G ENSP00000451560.1:p.Gly747=
NM_001197181.1:c.984C>G NP_001184110.1:p.Gly328=
NM_006086.3:c.1200C>G NP_006077.2:p.Gly400=
NM_006086.4:c.1200C>G MANE Select NP_006077.2:p.Gly400=
NM_001197181.2:c.984C>G NP_001184110.1:p.Gly328=