Canonical Allele Identifier: CA645163237
Gene: OPN1MW2 HGNC NCBI

Linked Data

dbSNP Id: rs1557161327
gnomAD v2: X-153496388-C-G
MyVariant Identifiers: chrX:g.153496388C>G (hg19) chrX:g.154230919C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154230919C>G , CM000685.2:g.154230919C>G GRCh38
NC_000023.10:g.153496388C>G , CM000685.1:g.153496388C>G GRCh37
NC_000023.9:g.153149582C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369929.8:c.984+132C>G MANE Select ENSP00000358945.4:n.984+132C>G
ENST00000430419.1:c.382+321C>G
NM_001048181.2:c.984+132C>G NP_001041646.1:n.984+132C>G
NM_001048181.3:c.984+132C>G MANE Select NP_001041646.1:n.984+132C>G
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