Canonical Allele Identifier: CA497381375
Gene: TUBB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.90001711G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935303G>C , CM000678.2:g.89935303G>C GRCh38
NC_000016.9:g.90001711G>C , CM000678.1:g.90001711G>C GRCh37
NC_000016.8:g.88529212G>C NCBI36
NG_027810.1:g.18295G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.852G>C MANE Select ENSP00000320295.7:p.Leu284=
ENST00000680788.1:n.4273G>C
ENST00000315491.11:c.852G>C ENSP00000320295.7:p.Leu284=
ENST00000554444.5:c.636G>C ENSP00000451617.1:p.Leu212=
ENST00000555576.5:c.277+1725G>C ENSP00000452554.1:n.277+1725G>C
ENST00000555609.5:c.*937G>C ENSP00000451276.1:n.*937G>C
ENST00000556922.1:c.1893G>C ENSP00000451560.1:p.Leu631=
NM_001197181.1:c.636G>C NP_001184110.1:p.Leu212=
NM_006086.3:c.852G>C NP_006077.2:p.Leu284=
NM_006086.4:c.852G>C MANE Select NP_006077.2:p.Leu284=
NM_001197181.2:c.636G>C NP_001184110.1:p.Leu212=