Canonical Allele Identifier: CA15041618
Gene: OPN1MW2 HGNC NCBI

Linked Data

dbSNP Id: rs5989620
gnomAD v2: X-153496355-G-A
MyVariant Identifiers: chrX:g.153496355G>A (hg19) chrX:g.154230886G>A (hg38)
PubMed: PMID:28263302
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154230886G>A , CM000685.2:g.154230886G>A GRCh38
NC_000023.10:g.153496355G>A , CM000685.1:g.153496355G>A GRCh37
NC_000023.9:g.153149549G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369929.8:c.984+99G>A MANE Select ENSP00000358945.4:n.984+99G>A
ENST00000430419.1:c.382+288G>A
NM_001048181.2:c.984+99G>A NP_001041646.1:n.984+99G>A
NM_001048181.3:c.984+99G>A MANE Select NP_001041646.1:n.984+99G>A
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