Canonical Allele Identifier: CA415312778
Gene: OPN1MW HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153453354A>T (hg19) chrX:g.154187865A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187865A>T , CM000685.2:g.154187865A>T GRCh38
NC_000023.10:g.153453354A>T , CM000685.1:g.153453354A>T GRCh37
NG_011606.1:g.10270A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000595290.6:c.208A>T MANE Select ENSP00000472316.1:p.Thr70Ser
ENST00000595290.5:c.208A>T ENSP00000472316.1:p.Thr70Ser
ENST00000595330.1:n.218A>T
NM_000513.2:c.208A>T MANE Select NP_000504.1:p.Thr70Ser
Search 100 bp 5'
Search 100 bp 3'