Canonical Allele Identifier: CA415309239
Gene: OPN1LW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153424328T>A (hg19) chrX:g.154158853T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154158853T>A , CM000685.2:g.154158853T>A GRCh38
NC_000023.10:g.153424328T>A , CM000685.1:g.153424328T>A GRCh37
NC_000023.9:g.153077522T>A NCBI36
NG_009105.2:g.19603T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369951.9:c.1022T>A MANE Select ENSP00000358967.4:p.Val341Asp
ENST00000369951.8:c.1022T>A ENSP00000358967.4:p.Val341Asp
ENST00000442922.1:c.422T>A ENSP00000402493.1:p.Val141Asp
NM_020061.5:c.1022T>A NP_064445.2:p.Val341Asp
NM_020061.6:c.1022T>A MANE Select NP_064445.2:p.Val341Asp
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