Canonical Allele Identifier: CA198640893
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs532482857
gnomAD v2: 9-117088095-G-A
gnomAD v3: 9-114325815-G-A
gnomAD v4: 9-114325815-G-A
MyVariant Identifiers: chr9:g.117088095G>A (hg19) chr9:g.114325815G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325815G>A , CM000671.2:g.114325815G>A GRCh38
NC_000009.11:g.117088095G>A , CM000671.1:g.117088095G>A GRCh37
NC_000009.10:g.116127916G>A NCBI36
NG_012108.1:g.7793G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-477G>A MANE Select ENSP00000259396.8:n.541-477G>A
ENST00000259396.8:c.541-477G>A ENSP00000259396.8:n.541-477G>A
NM_000607.2:c.541-477G>A NP_000598.2:n.541-477G>A
NM_000607.3:c.541-477G>A NP_000598.2:n.541-477G>A
NM_000607.4:c.541-477G>A MANE Select NP_000598.2:n.541-477G>A
Search 100 bp 5'
Search 100 bp 3'