Canonical Allele Identifier: CA2529568171
Gene: OPN1MW HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191542T>G , CM000685.2:g.154191542T>G GRCh38
NC_000023.10:g.153457033T>G , CM000685.1:g.153457033T>G GRCh37
NG_011606.1:g.13949T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.579-146T>G MANE Select ENSP00000472316.1:n.579-146T>G
ENST00000595290.5:c.579-146T>G ENSP00000472316.1:n.579-146T>G
ENST00000595330.1:n.588+1320T>G
ENST00000596998.2:c.166-146T>G
NM_000513.2:c.579-146T>G MANE Select NP_000504.1:n.579-146T>G