Canonical Allele Identifier: CA415313179
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453423G>C (hg19) chrX:g.154187934G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187934G>C , CM000685.2:g.154187934G>C GRCh38
NC_000023.10:g.153453423G>C , CM000685.1:g.153453423G>C GRCh37
NG_011606.1:g.10339G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.277G>C MANE Select ENSP00000472316.1:p.Val93Leu
ENST00000595290.5:c.277G>C ENSP00000472316.1:p.Val93Leu
ENST00000595330.1:n.287G>C
NM_000513.2:c.277G>C MANE Select NP_000504.1:p.Val93Leu
Search 100 bp 5'
Search 100 bp 3'