Canonical Allele Identifier: CA519324125
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424326G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158851G>A , CM000685.2:g.154158851G>A GRCh38
NC_000023.10:g.153424326G>A , CM000685.1:g.153424326G>A GRCh37
NC_000023.9:g.153077520G>A NCBI36
NG_009105.2:g.19601G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1020G>A MANE Select ENSP00000358967.4:p.Lys340=
ENST00000369951.8:c.1020G>A ENSP00000358967.4:p.Lys340=
ENST00000442922.1:c.420G>A ENSP00000402493.1:p.Lys140=
NM_020061.5:c.1020G>A NP_064445.2:p.Lys340=
NM_020061.6:c.1020G>A MANE Select NP_064445.2:p.Lys340=
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Search 100 bp 3'