Canonical Allele Identifier: CA415312766

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453351T>C (hg19) ; chrX:g.154187862T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187862T>C , CM000685.2:g.154187862T>C	GRCh38
NC_000023.10:g.153453351T>C , CM000685.1:g.153453351T>C	GRCh37
NG_011606.1:g.10267T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.205T>C MANE Select	ENSP00000472316.1:p.Phe69Leu
ENST00000595290.5:c.205T>C	ENSP00000472316.1:p.Phe69Leu
ENST00000595330.1:n.215T>C
NM_000513.2:c.205T>C MANE Select	NP_000504.1:p.Phe69Leu