Canonical Allele Identifier: CA415312772
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453352T>G (hg19) chrX:g.154187863T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187863T>G , CM000685.2:g.154187863T>G GRCh38
NC_000023.10:g.153453352T>G , CM000685.1:g.153453352T>G GRCh37
NG_011606.1:g.10268T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.206T>G MANE Select ENSP00000472316.1:p.Phe69Cys
ENST00000595290.5:c.206T>G ENSP00000472316.1:p.Phe69Cys
ENST00000595330.1:n.216T>G
NM_000513.2:c.206T>G MANE Select NP_000504.1:p.Phe69Cys
Search 100 bp 5'
Search 100 bp 3'