Canonical Allele Identifier: CA2466617942
Gene: OPN1MW HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191555G= , CM000685.2:g.154191555G= GRCh38
NC_000023.10:g.153457046G= , CM000685.1:g.153457046G= GRCh37
NG_011606.1:g.13962G=

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.579-133G= MANE Select ENSP00000472316.1:n.579-133G=
ENST00000595290.5:c.579-133G= ENSP00000472316.1:n.579-133G=
ENST00000595330.1:n.588+1333G=
ENST00000596998.2:c.166-133G=
NM_000513.2:c.579-133G= MANE Select NP_000504.1:n.579-133G=
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