Canonical Allele Identifier: CA519323119
Gene: OPN1LW HGNC NCBI

Linked Data

gnomAD v4: X-154154734-C-A
MyVariant Identifiers: chrX:g.153420209C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154154734C>A , CM000685.2:g.154154734C>A GRCh38
NC_000023.10:g.153420209C>A , CM000685.1:g.153420209C>A GRCh37
NC_000023.9:g.153073403C>A NCBI36
NG_009105.2:g.15484C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.739C>A MANE Select ENSP00000358967.4:p.Arg247=
ENST00000369951.8:c.739C>A ENSP00000358967.4:p.Arg247=
ENST00000442922.1:c.328C>A ENSP00000402493.1:p.Arg110=
ENST00000463296.1:n.589-1560C>A
NM_020061.5:c.739C>A NP_064445.2:p.Arg247=
NM_020061.6:c.739C>A MANE Select NP_064445.2:p.Arg247=
Search 100 bp 5'
Search 100 bp 3'