Canonical Allele Identifier: CA415306299

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153420111C>T (hg19) ; chrX:g.154154636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154154636C>T , CM000685.2:g.154154636C>T	GRCh38
NC_000023.10:g.153420111C>T , CM000685.1:g.153420111C>T	GRCh37
NC_000023.9:g.153073305C>T	NCBI36
NG_009105.2:g.15386C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.641C>T MANE Select	ENSP00000358967.4:p.Pro214Leu
ENST00000369951.8:c.641C>T	ENSP00000358967.4:p.Pro214Leu
ENST00000442922.1:c.230C>T	ENSP00000402493.1:p.Pro77Leu
ENST00000463296.1:n.588+1528C>T
NM_020061.5:c.641C>T	NP_064445.2:p.Pro214Leu
NM_020061.6:c.641C>T MANE Select	NP_064445.2:p.Pro214Leu