Canonical Allele Identifier: CA519323025
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153420112C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154154637C>A , CM000685.2:g.154154637C>A GRCh38
NC_000023.10:g.153420112C>A , CM000685.1:g.153420112C>A GRCh37
NC_000023.9:g.153073306C>A NCBI36
NG_009105.2:g.15387C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.642C>A MANE Select ENSP00000358967.4:p.Pro214=
ENST00000369951.8:c.642C>A ENSP00000358967.4:p.Pro214=
ENST00000442922.1:c.231C>A ENSP00000402493.1:p.Pro77=
ENST00000463296.1:n.588+1529C>A
NM_020061.5:c.642C>A NP_064445.2:p.Pro214=
NM_020061.6:c.642C>A MANE Select NP_064445.2:p.Pro214=
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