Canonical Allele Identifier: CA415309222

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153424322A>G (hg19) ; chrX:g.154158847A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154158847A>G , CM000685.2:g.154158847A>G	GRCh38
NC_000023.10:g.153424322A>G , CM000685.1:g.153424322A>G	GRCh37
NC_000023.9:g.153077516A>G	NCBI36
NG_009105.2:g.19597A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.1016A>G MANE Select	ENSP00000358967.4:p.Lys339Arg
ENST00000369951.8:c.1016A>G	ENSP00000358967.4:p.Lys339Arg
ENST00000442922.1:c.416A>G	ENSP00000402493.1:p.Lys139Arg
NM_020061.5:c.1016A>G	NP_064445.2:p.Lys339Arg
NM_020061.6:c.1016A>G MANE Select	NP_064445.2:p.Lys339Arg