Canonical Allele Identifier: CA415314629
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153457182C>A (hg19) chrX:g.154191691C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191691C>A , CM000685.2:g.154191691C>A GRCh38
NC_000023.10:g.153457182C>A , CM000685.1:g.153457182C>A GRCh37
NG_011606.1:g.14098C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.582C>A MANE Select ENSP00000472316.1:p.Tyr194Ter
ENST00000595290.5:c.582C>A ENSP00000472316.1:p.Tyr194Ter
ENST00000595330.1:n.588+1469C>A
ENST00000596998.2:c.169C>A
NM_000513.2:c.582C>A MANE Select NP_000504.1:p.Tyr194Ter
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