Canonical Allele Identifier: CA415312687

Gene: OPN1MW

Linked Data

• MyVariant Identifiers: chrX:g.153453331T>C (hg19) ; chrX:g.154187842T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154187842T>C , CM000685.2:g.154187842T>C	GRCh38
NC_000023.10:g.153453331T>C , CM000685.1:g.153453331T>C	GRCh37
NG_011606.1:g.10247T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000595290.6:c.185T>C MANE Select	ENSP00000472316.1:p.Phe62Ser
ENST00000595290.5:c.185T>C	ENSP00000472316.1:p.Phe62Ser
ENST00000595330.1:n.195T>C
NM_000513.2:c.185T>C MANE Select	NP_000504.1:p.Phe62Ser