Canonical Allele Identifier: CA10558947
Gene: OPN1MW HGNC NCBI

Linked Data

dbSNP Id: rs782712624

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187918G>A , CM000685.2:g.154187918G>A GRCh38
NC_000023.10:g.153453407G>A , CM000685.1:g.153453407G>A GRCh37
NG_011606.1:g.10323G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.261G>A MANE Select ENSP00000472316.1:p.Pro87=
ENST00000595290.5:c.261G>A ENSP00000472316.1:p.Pro87=
ENST00000595330.1:n.271G>A
NM_000513.2:c.261G>A MANE Select NP_000504.1:p.Pro87=