Canonical Allele Identifier: CA858953522
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1160739709
gnomAD v3: 9-114325825-C-A
gnomAD v4: 9-114325825-C-A
MyVariant Identifiers: chr9:g.117088105C>A (hg19) chr9:g.114325825C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325825C>A , CM000671.2:g.114325825C>A GRCh38
NC_000009.11:g.117088105C>A , CM000671.1:g.117088105C>A GRCh37
NC_000009.10:g.116127926C>A NCBI36
NG_012108.1:g.7803C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-467C>A MANE Select ENSP00000259396.8:n.541-467C>A
ENST00000259396.8:c.541-467C>A ENSP00000259396.8:n.541-467C>A
NM_000607.2:c.541-467C>A NP_000598.2:n.541-467C>A
NM_000607.3:c.541-467C>A NP_000598.2:n.541-467C>A
NM_000607.4:c.541-467C>A MANE Select NP_000598.2:n.541-467C>A
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