Canonical Allele Identifier: CA415312780

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453354A>C (hg19) ; chrX:g.154187865A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187865A>C , CM000685.2:g.154187865A>C	GRCh38
NC_000023.10:g.153453354A>C , CM000685.1:g.153453354A>C	GRCh37
NG_011606.1:g.10270A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.208A>C MANE Select	ENSP00000472316.1:p.Thr70Pro
ENST00000595290.5:c.208A>C	ENSP00000472316.1:p.Thr70Pro
ENST00000595330.1:n.218A>C
NM_000513.2:c.208A>C MANE Select	NP_000504.1:p.Thr70Pro