Canonical Allele Identifier: CA519324128

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153424329T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154158854T>G , CM000685.2:g.154158854T>G	GRCh38
NC_000023.10:g.153424329T>G , CM000685.1:g.153424329T>G	GRCh37
NC_000023.9:g.153077523T>G	NCBI36
NG_009105.2:g.19604T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.1023T>G MANE Select	ENSP00000358967.4:p.Val341=
ENST00000369951.8:c.1023T>G	ENSP00000358967.4:p.Val341=
ENST00000442922.1:c.423T>G	ENSP00000402493.1:p.Val141=
NM_020061.5:c.1023T>G	NP_064445.2:p.Val341=
NM_020061.6:c.1023T>G MANE Select	NP_064445.2:p.Val341=