Canonical Allele Identifier: CA415313253
Gene: OPN1MW HGNC NCBI

Linked Data

gnomAD v4: X-154187947-T-A
MyVariant Identifiers: chrX:g.153453436T>A (hg19) chrX:g.154187947T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187947T>A , CM000685.2:g.154187947T>A GRCh38
NC_000023.10:g.153453436T>A , CM000685.1:g.153453436T>A GRCh37
NG_011606.1:g.10352T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.290T>A MANE Select ENSP00000472316.1:p.Val97Asp
ENST00000595290.5:c.290T>A ENSP00000472316.1:p.Val97Asp
ENST00000595330.1:n.300T>A
NM_000513.2:c.290T>A MANE Select NP_000504.1:p.Val97Asp
Search 100 bp 5'
Search 100 bp 3'