Canonical Allele Identifier: CA519716345
Gene: OPN1MW HGNC NCBI

Linked Data

dbSNP Id: rs1353157525
gnomAD v2: X-153453380-C-G
gnomAD v3: X-154187891-C-G
gnomAD v4: X-154187891-C-G
MyVariant Identifiers: chrX:g.153453380C>G (hg19) chrX:g.154187891C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154187891C>G , CM000685.2:g.154187891C>G GRCh38
NC_000023.10:g.153453380C>G , CM000685.1:g.153453380C>G GRCh37
NG_011606.1:g.10296C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000595290.6:c.234C>G MANE Select ENSP00000472316.1:p.Thr78=
ENST00000595290.5:c.234C>G ENSP00000472316.1:p.Thr78=
ENST00000595330.1:n.244C>G
NM_000513.2:c.234C>G MANE Select NP_000504.1:p.Thr78=
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