Canonical Allele Identifier: CA590134265
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1267662623
gnomAD v2: 9-117088089-C-A
gnomAD v3: 9-114325809-C-A
gnomAD v4: 9-114325809-C-A
MyVariant Identifiers: chr9:g.117088089C>A (hg19) chr9:g.114325809C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325809C>A , CM000671.2:g.114325809C>A GRCh38
NC_000009.11:g.117088089C>A , CM000671.1:g.117088089C>A GRCh37
NC_000009.10:g.116127910C>A NCBI36
NG_012108.1:g.7787C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-483C>A MANE Select ENSP00000259396.8:n.541-483C>A
ENST00000259396.8:c.541-483C>A ENSP00000259396.8:n.541-483C>A
NM_000607.2:c.541-483C>A NP_000598.2:n.541-483C>A
NM_000607.3:c.541-483C>A NP_000598.2:n.541-483C>A
NM_000607.4:c.541-483C>A MANE Select NP_000598.2:n.541-483C>A
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