Canonical Allele Identifier: CA519324101
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424320G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158845G>A , CM000685.2:g.154158845G>A GRCh38
NC_000023.10:g.153424320G>A , CM000685.1:g.153424320G>A GRCh37
NC_000023.9:g.153077514G>A NCBI36
NG_009105.2:g.19595G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1014G>A MANE Select ENSP00000358967.4:p.Gly338=
ENST00000369951.8:c.1014G>A ENSP00000358967.4:p.Gly338=
ENST00000442922.1:c.414G>A ENSP00000402493.1:p.Gly138=
NM_020061.5:c.1014G>A NP_064445.2:p.Gly338=
NM_020061.6:c.1014G>A MANE Select NP_064445.2:p.Gly338=
Search 100 bp 5'
Search 100 bp 3'