Canonical Allele Identifier: CA519324118
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424323G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158848G>A , CM000685.2:g.154158848G>A GRCh38
NC_000023.10:g.153424323G>A , CM000685.1:g.153424323G>A GRCh37
NC_000023.9:g.153077517G>A NCBI36
NG_009105.2:g.19598G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1017G>A MANE Select ENSP00000358967.4:p.Lys339=
ENST00000369951.8:c.1017G>A ENSP00000358967.4:p.Lys339=
ENST00000442922.1:c.417G>A ENSP00000402493.1:p.Lys139=
NM_020061.5:c.1017G>A NP_064445.2:p.Lys339=
NM_020061.6:c.1017G>A MANE Select NP_064445.2:p.Lys339=
Search 100 bp 5'
Search 100 bp 3'