Canonical Allele Identifier: CA415314691
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153457209C>G (hg19) chrX:g.154191718C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191718C>G , CM000685.2:g.154191718C>G GRCh38
NC_000023.10:g.153457209C>G , CM000685.1:g.153457209C>G GRCh37
NG_011606.1:g.14125C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.609C>G MANE Select ENSP00000472316.1:p.Cys203Trp
ENST00000595290.5:c.609C>G ENSP00000472316.1:p.Cys203Trp
ENST00000595330.1:n.588+1496C>G
ENST00000596998.2:c.196C>G
NM_000513.2:c.609C>G MANE Select NP_000504.1:p.Cys203Trp
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