Canonical Allele Identifier: CA415309236
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424327G>A (hg19) chrX:g.154158852G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158852G>A , CM000685.2:g.154158852G>A GRCh38
NC_000023.10:g.153424327G>A , CM000685.1:g.153424327G>A GRCh37
NC_000023.9:g.153077521G>A NCBI36
NG_009105.2:g.19602G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1021G>A MANE Select ENSP00000358967.4:p.Val341Ile
ENST00000369951.8:c.1021G>A ENSP00000358967.4:p.Val341Ile
ENST00000442922.1:c.421G>A ENSP00000402493.1:p.Val141Ile
NM_020061.5:c.1021G>A NP_064445.2:p.Val341Ile
NM_020061.6:c.1021G>A MANE Select NP_064445.2:p.Val341Ile
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