Canonical Allele Identifier: CA415313014

Gene: OPN1MW

Linked Data

• dbSNP Id: rs2067108630
• gnomAD v3: X-154187911-G-A
• gnomAD v4: X-154187911-G-A
• MyVariant Identifiers: chrX:g.153453400G>A (hg19) ; chrX:g.154187911G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187911G>A , CM000685.2:g.154187911G>A	GRCh38
NC_000023.10:g.153453400G>A , CM000685.1:g.153453400G>A	GRCh37
NG_011606.1:g.10316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.254G>A MANE Select	ENSP00000472316.1:p.Arg85His
ENST00000595290.5:c.254G>A	ENSP00000472316.1:p.Arg85His
ENST00000595330.1:n.264G>A
NM_000513.2:c.254G>A MANE Select	NP_000504.1:p.Arg85His