Canonical Allele Identifier: CA645163240
Gene: OPN1MW2 HGNC NCBI

Linked Data

dbSNP Id: rs1557161330
gnomAD v2: X-153496430-C-T
MyVariant Identifiers: chrX:g.153496430C>T (hg19) chrX:g.154230961C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154230961C>T , CM000685.2:g.154230961C>T GRCh38
NC_000023.10:g.153496430C>T , CM000685.1:g.153496430C>T GRCh37
NC_000023.9:g.153149624C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369929.8:c.984+174C>T MANE Select ENSP00000358945.4:n.984+174C>T
ENST00000430419.1:c.382+363C>T
NM_001048181.2:c.984+174C>T NP_001041646.1:n.984+174C>T
NM_001048181.3:c.984+174C>T MANE Select NP_001041646.1:n.984+174C>T
Search 100 bp 5'
Search 100 bp 3'