Canonical Allele Identifier: CA415307423
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153420210G>C (hg19) chrX:g.154154735G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154154735G>C , CM000685.2:g.154154735G>C GRCh38
NC_000023.10:g.153420210G>C , CM000685.1:g.153420210G>C GRCh37
NC_000023.9:g.153073404G>C NCBI36
NG_009105.2:g.15485G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.740G>C MANE Select ENSP00000358967.4:p.Arg247Pro
ENST00000369951.8:c.740G>C ENSP00000358967.4:p.Arg247Pro
ENST00000442922.1:c.329G>C ENSP00000402493.1:p.Arg110Pro
ENST00000463296.1:n.589-1559G>C
NM_020061.5:c.740G>C NP_064445.2:p.Arg247Pro
NM_020061.6:c.740G>C MANE Select NP_064445.2:p.Arg247Pro
Search 100 bp 5'
Search 100 bp 3'