Canonical Allele Identifier: CA519716387
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453440T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187951T>A , CM000685.2:g.154187951T>A GRCh38
NC_000023.10:g.153453440T>A , CM000685.1:g.153453440T>A GRCh37
NG_011606.1:g.10356T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.294T>A MANE Select ENSP00000472316.1:p.Ala98=
ENST00000595290.5:c.294T>A ENSP00000472316.1:p.Ala98=
ENST00000595330.1:n.304T>A
NM_000513.2:c.294T>A MANE Select NP_000504.1:p.Ala98=
Search 100 bp 5'
Search 100 bp 3'