Canonical Allele Identifier: CA10558824
Gene: OPN1LW HGNC NCBI

Linked Data

ClinVar Variation Id: 403267
ClinVar RCV Id: RCV000454776
dbSNP Id: rs145009674
ExAC: X:153418535 A / G
gnomAD v2: X-153418535-A-G
MyVariant Identifiers: chrX:g.153418535A>G (hg19) chrX:g.154153062A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154153062A>G , CM000685.2:g.154153062A>G GRCh38
NC_000023.10:g.153418535A>G , CM000685.1:g.153418535A>G GRCh37
NC_000023.9:g.153071729A>G NCBI36
NG_009105.2:g.13812A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369951.9:c.532A>G MANE Select ENSP00000358967.4:p.Ile178Val
ENST00000369951.8:c.532A>G ENSP00000358967.4:p.Ile178Val
ENST00000442922.1:c.121A>G ENSP00000402493.1:p.Ile41Val
ENST00000463296.1:n.542A>G
NM_020061.5:c.532A>G NP_064445.2:p.Ile178Val
NM_020061.6:c.532A>G MANE Select NP_064445.2:p.Ile178Val
Search 100 bp 5'
Search 100 bp 3'