Canonical Allele Identifier: CA415307481

Gene: OPN1LW

Linked Data

• MyVariant Identifiers: chrX:g.153420216T>C (hg19) ; chrX:g.154154741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154154741T>C , CM000685.2:g.154154741T>C	GRCh38
NC_000023.10:g.153420216T>C , CM000685.1:g.153420216T>C	GRCh37
NC_000023.9:g.153073410T>C	NCBI36
NG_009105.2:g.15491T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369951.9:c.744+2T>C MANE Select	ENSP00000358967.4:n.744+2T>C
ENST00000369951.8:c.744+2T>C	ENSP00000358967.4:n.744+2T>C
ENST00000442922.1:c.333+2T>C	ENSP00000402493.1:n.333+2T>C
ENST00000463296.1:n.589-1553T>C
NM_020061.5:c.744+2T>C	NP_064445.2:n.744+2T>C
NM_020061.6:c.744+2T>C MANE Select	NP_064445.2:n.744+2T>C