Canonical Allele Identifier: CA519324129

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153424332C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154158857C>T , CM000685.2:g.154158857C>T	GRCh38
NC_000023.10:g.153424332C>T , CM000685.1:g.153424332C>T	GRCh37
NC_000023.9:g.153077526C>T	NCBI36
NG_009105.2:g.19607C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.1026C>T MANE Select	ENSP00000358967.4:p.Asp342=
ENST00000369951.8:c.1026C>T	ENSP00000358967.4:p.Asp342=
ENST00000442922.1:c.426C>T	ENSP00000402493.1:p.Asp142=
NM_020061.5:c.1026C>T	NP_064445.2:p.Asp342=
NM_020061.6:c.1026C>T MANE Select	NP_064445.2:p.Asp342=