Canonical Allele Identifier: CA415313759

Gene: OPN1MW

Linked Data

• gnomAD v4: X-154188025-A-G
• MyVariant Identifiers: chrX:g.153453514A>G (hg19) ; chrX:g.154188025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154188025A>G , CM000685.2:g.154188025A>G	GRCh38
NC_000023.10:g.153453514A>G , CM000685.1:g.153453514A>G	GRCh37
NG_011606.1:g.10430A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.368A>G MANE Select	ENSP00000472316.1:p.His123Arg
ENST00000595290.5:c.368A>G	ENSP00000472316.1:p.His123Arg
ENST00000595330.1:n.378A>G
NM_000513.2:c.368A>G MANE Select	NP_000504.1:p.His123Arg