Canonical Allele Identifier: CA415309238

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153424327G>T (hg19) ; chrX:g.154158852G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154158852G>T , CM000685.2:g.154158852G>T	GRCh38
NC_000023.10:g.153424327G>T , CM000685.1:g.153424327G>T	GRCh37
NC_000023.9:g.153077521G>T	NCBI36
NG_009105.2:g.19602G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.1021G>T MANE Select	ENSP00000358967.4:p.Val341Phe
ENST00000369951.8:c.1021G>T	ENSP00000358967.4:p.Val341Phe
ENST00000442922.1:c.421G>T	ENSP00000402493.1:p.Val141Phe
NM_020061.5:c.1021G>T	NP_064445.2:p.Val341Phe
NM_020061.6:c.1021G>T MANE Select	NP_064445.2:p.Val341Phe