Canonical Allele Identifier: CA415313466

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453468A>C (hg19) ; chrX:g.154187979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187979A>C , CM000685.2:g.154187979A>C	GRCh38
NC_000023.10:g.153453468A>C , CM000685.1:g.153453468A>C	GRCh37
NG_011606.1:g.10384A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.322A>C MANE Select	ENSP00000472316.1:p.Thr108Pro
ENST00000595290.5:c.322A>C	ENSP00000472316.1:p.Thr108Pro
ENST00000595330.1:n.332A>C
NM_000513.2:c.322A>C MANE Select	NP_000504.1:p.Thr108Pro