Canonical Allele Identifier: CA10558955
Gene: OPN1MW HGNC NCBI

Linked Data

dbSNP Id: rs782460974
ExAC: X:153453455 C / T
gnomAD v2: X-153453455-C-T
gnomAD v3: X-154187966-C-T
gnomAD v4: X-154187966-C-T
MyVariant Identifiers: chrX:g.153453455C>T (hg19) chrX:g.154187966C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187966C>T , CM000685.2:g.154187966C>T GRCh38
NC_000023.10:g.153453455C>T , CM000685.1:g.153453455C>T GRCh37
NG_011606.1:g.10371C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.309C>T MANE Select ENSP00000472316.1:p.Thr103=
ENST00000595290.5:c.309C>T ENSP00000472316.1:p.Thr103=
ENST00000595330.1:n.319C>T
NM_000513.2:c.309C>T MANE Select NP_000504.1:p.Thr103=
Search 100 bp 5'
Search 100 bp 3'