Canonical Allele Identifier: CA415313737

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453510G>A (hg19) ; chrX:g.154188021G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154188021G>A , CM000685.2:g.154188021G>A	GRCh38
NC_000023.10:g.153453510G>A , CM000685.1:g.153453510G>A	GRCh37
NG_011606.1:g.10426G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595290.6:c.364G>A MANE Select	ENSP00000472316.1:p.Gly122Ser
ENST00000595290.5:c.364G>A	ENSP00000472316.1:p.Gly122Ser
ENST00000595330.1:n.374G>A
NM_000513.2:c.364G>A MANE Select	NP_000504.1:p.Gly122Ser