Canonical Allele Identifier: CA415313466
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453468A>C (hg19) chrX:g.154187979A>C (hg38)
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'