Canonical Allele Identifier: CA497381080
Gene: TUBB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.90001543G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935135G>T , CM000678.2:g.89935135G>T GRCh38
NC_000016.9:g.90001543G>T , CM000678.1:g.90001543G>T GRCh37
NC_000016.8:g.88529044G>T NCBI36
NG_027810.1:g.18127G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000315491.12:c.684G>T MANE Select ENSP00000320295.7:p.Leu228=
ENST00000680788.1:n.4105G>T
ENST00000315491.11:c.684G>T ENSP00000320295.7:p.Leu228=
ENST00000554444.5:c.468G>T ENSP00000451617.1:p.Leu156=
ENST00000555576.5:c.277+1557G>T ENSP00000452554.1:n.277+1557G>T
ENST00000555609.5:c.*769G>T ENSP00000451276.1:n.*769G>T
ENST00000555810.5:c.468G>T ENSP00000450538.1:p.Leu156=
ENST00000556922.1:c.1725G>T ENSP00000451560.1:p.Leu575=
NM_001197181.1:c.468G>T NP_001184110.1:p.Leu156=
NM_006086.3:c.684G>T NP_006077.2:p.Leu228=
NM_006086.4:c.684G>T MANE Select NP_006077.2:p.Leu228=
NM_001197181.2:c.468G>T NP_001184110.1:p.Leu156=