Canonical Allele Identifier: CA519716368
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453413C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187924C>T , CM000685.2:g.154187924C>T GRCh38
NC_000023.10:g.153453413C>T , CM000685.1:g.153453413C>T GRCh37
NG_011606.1:g.10329C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.267C>T MANE Select ENSP00000472316.1:p.Asn89=
ENST00000595290.5:c.267C>T ENSP00000472316.1:p.Asn89=
ENST00000595330.1:n.277C>T
NM_000513.2:c.267C>T MANE Select NP_000504.1:p.Asn89=
Search 100 bp 5'
Search 100 bp 3'