Canonical Allele Identifier: CA497194423
Gene: TUBB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.90002035G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935627G>A , CM000678.2:g.89935627G>A GRCh38
NC_000016.9:g.90002035G>A , CM000678.1:g.90002035G>A GRCh37
NC_000016.8:g.88529536G>A NCBI36
NG_027810.1:g.18619G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.1176G>A MANE Select ENSP00000320295.7:p.Lys392=
ENST00000680788.1:n.4597G>A
ENST00000315491.11:c.1176G>A ENSP00000320295.7:p.Lys392=
ENST00000554444.5:c.960G>A ENSP00000451617.1:p.Lys320=
ENST00000555576.5:c.277+2049G>A ENSP00000452554.1:n.277+2049G>A
ENST00000555609.5:c.*1261G>A ENSP00000451276.1:n.*1261G>A
ENST00000556922.1:c.2217G>A ENSP00000451560.1:p.Lys739=
NM_001197181.1:c.960G>A NP_001184110.1:p.Lys320=
NM_006086.3:c.1176G>A NP_006077.2:p.Lys392=
NM_006086.4:c.1176G>A MANE Select NP_006077.2:p.Lys392=
NM_001197181.2:c.960G>A NP_001184110.1:p.Lys320=