Canonical Allele Identifier: CA2466622851
Gene: OPN1MW2 HGNC NCBI

Linked Data

dbSNP Id: rs1603348299

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154230968C>G , CM000685.2:g.154230968C>G GRCh38
NC_000023.10:g.153496437C>G , CM000685.1:g.153496437C>G GRCh37
NC_000023.9:g.153149631C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369929.8:c.984+181C>G MANE Select ENSP00000358945.4:n.984+181C>G
ENST00000430419.1:c.382+370C>G
NM_001048181.2:c.984+181C>G NP_001041646.1:n.984+181C>G
NM_001048181.3:c.984+181C>G MANE Select NP_001041646.1:n.984+181C>G