Canonical Allele Identifier: CA415313217
Gene: OPN1MW HGNC NCBI

Linked Data

gnomAD v4: X-154187941-T-G
MyVariant Identifiers: chrX:g.153453430T>G (hg19) chrX:g.154187941T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187941T>G , CM000685.2:g.154187941T>G GRCh38
NC_000023.10:g.153453430T>G , CM000685.1:g.153453430T>G GRCh37
NG_011606.1:g.10346T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.284T>G MANE Select ENSP00000472316.1:p.Leu95Arg
ENST00000595290.5:c.284T>G ENSP00000472316.1:p.Leu95Arg
ENST00000595330.1:n.294T>G
NM_000513.2:c.284T>G MANE Select NP_000504.1:p.Leu95Arg
Search 100 bp 5'
Search 100 bp 3'