Canonical Allele Identifier: CA415314632
Gene: OPN1MW HGNC NCBI

Linked Data

gnomAD v4: X-154191692-T-C
MyVariant Identifiers: chrX:g.153457183T>C (hg19) chrX:g.154191692T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191692T>C , CM000685.2:g.154191692T>C GRCh38
NC_000023.10:g.153457183T>C , CM000685.1:g.153457183T>C GRCh37
NG_011606.1:g.14099T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.583T>C MANE Select ENSP00000472316.1:p.Trp195Arg
ENST00000595290.5:c.583T>C ENSP00000472316.1:p.Trp195Arg
ENST00000595330.1:n.588+1470T>C
ENST00000596998.2:c.170T>C
NM_000513.2:c.583T>C MANE Select NP_000504.1:p.Trp195Arg
Search 100 bp 5'
Search 100 bp 3'