Canonical Allele Identifier: CA519716393
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453449A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187960A>C , CM000685.2:g.154187960A>C GRCh38
NC_000023.10:g.153453449A>C , CM000685.1:g.153453449A>C GRCh37
NG_011606.1:g.10365A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.303A>C MANE Select ENSP00000472316.1:p.Ala101=
ENST00000595290.5:c.303A>C ENSP00000472316.1:p.Ala101=
ENST00000595330.1:n.313A>C
NM_000513.2:c.303A>C MANE Select NP_000504.1:p.Ala101=