Canonical Allele Identifier: CA415314708
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153457217A>G (hg19) chrX:g.154191726A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154191726A>G , CM000685.2:g.154191726A>G GRCh38
NC_000023.10:g.153457217A>G , CM000685.1:g.153457217A>G GRCh37
NG_011606.1:g.14133A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.617A>G MANE Select ENSP00000472316.1:p.Asp206Gly
ENST00000595290.5:c.617A>G ENSP00000472316.1:p.Asp206Gly
ENST00000595330.1:n.588+1504A>G
ENST00000596998.2:c.204A>G
NM_000513.2:c.617A>G MANE Select NP_000504.1:p.Asp206Gly
Search 100 bp 5'
Search 100 bp 3'