Canonical Allele Identifier: CA415312667

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453328T>G (hg19) ; chrX:g.154187839T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187839T>G , CM000685.2:g.154187839T>G	GRCh38
NC_000023.10:g.153453328T>G , CM000685.1:g.153453328T>G	GRCh37
NG_011606.1:g.10244T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000595290.6:c.182T>G MANE Select	ENSP00000472316.1:p.Ile61Ser
ENST00000595290.5:c.182T>G	ENSP00000472316.1:p.Ile61Ser
ENST00000595330.1:n.192T>G
NM_000513.2:c.182T>G MANE Select	NP_000504.1:p.Ile61Ser