Canonical Allele Identifier: CA2824290657
Gene: OPN1MW HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191678T>G , CM000685.2:g.154191678T>G GRCh38
NC_000023.10:g.153457169T>G , CM000685.1:g.153457169T>G GRCh37
NG_011606.1:g.14085T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.579-10T>G MANE Select ENSP00000472316.1:n.579-10T>G
ENST00000595290.5:c.579-10T>G ENSP00000472316.1:n.579-10T>G
ENST00000595330.1:n.588+1456T>G
ENST00000596998.2:c.166-10T>G
NM_000513.2:c.579-10T>G MANE Select NP_000504.1:n.579-10T>G