Canonical Allele Identifier: CA415313911
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453544T>G (hg19) chrX:g.154188055T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154188055T>G , CM000685.2:g.154188055T>G GRCh38
NC_000023.10:g.153453544T>G , CM000685.1:g.153453544T>G GRCh37
NG_011606.1:g.10460T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.398T>G MANE Select ENSP00000472316.1:p.Val133Gly
ENST00000595290.5:c.398T>G ENSP00000472316.1:p.Val133Gly
ENST00000595330.1:n.408T>G
NM_000513.2:c.398T>G MANE Select NP_000504.1:p.Val133Gly
Search 100 bp 5'
Search 100 bp 3'