Canonical Allele Identifier: CA415309216
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424319G>C (hg19) chrX:g.154158844G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158844G>C , CM000685.2:g.154158844G>C GRCh38
NC_000023.10:g.153424319G>C , CM000685.1:g.153424319G>C GRCh37
NC_000023.9:g.153077513G>C NCBI36
NG_009105.2:g.19594G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1013G>C MANE Select ENSP00000358967.4:p.Gly338Ala
ENST00000369951.8:c.1013G>C ENSP00000358967.4:p.Gly338Ala
ENST00000442922.1:c.413G>C ENSP00000402493.1:p.Gly138Ala
NM_020061.5:c.1013G>C NP_064445.2:p.Gly338Ala
NM_020061.6:c.1013G>C MANE Select NP_064445.2:p.Gly338Ala
Search 100 bp 5'
Search 100 bp 3'