Canonical Allele Identifier: CA590134264
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1206890797
gnomAD v2: 9-117088088-A-G
gnomAD v3: 9-114325808-A-G
gnomAD v4: 9-114325808-A-G
MyVariant Identifiers: chr9:g.117088088A>G (hg19) chr9:g.114325808A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325808A>G , CM000671.2:g.114325808A>G GRCh38
NC_000009.11:g.117088088A>G , CM000671.1:g.117088088A>G GRCh37
NC_000009.10:g.116127909A>G NCBI36
NG_012108.1:g.7786A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-484A>G MANE Select ENSP00000259396.8:n.541-484A>G
ENST00000259396.8:c.541-484A>G ENSP00000259396.8:n.541-484A>G
NM_000607.2:c.541-484A>G NP_000598.2:n.541-484A>G
NM_000607.3:c.541-484A>G NP_000598.2:n.541-484A>G
NM_000607.4:c.541-484A>G MANE Select NP_000598.2:n.541-484A>G
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