Canonical Allele Identifier: CA858953521
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1415077155
gnomAD v3: 9-114325821-A-T
gnomAD v4: 9-114325821-A-T
MyVariant Identifiers: chr9:g.117088101A>T (hg19) chr9:g.114325821A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325821A>T , CM000671.2:g.114325821A>T GRCh38
NC_000009.11:g.117088101A>T , CM000671.1:g.117088101A>T GRCh37
NC_000009.10:g.116127922A>T NCBI36
NG_012108.1:g.7799A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-471A>T MANE Select ENSP00000259396.8:n.541-471A>T
ENST00000259396.8:c.541-471A>T ENSP00000259396.8:n.541-471A>T
NM_000607.2:c.541-471A>T NP_000598.2:n.541-471A>T
NM_000607.3:c.541-471A>T NP_000598.2:n.541-471A>T
NM_000607.4:c.541-471A>T MANE Select NP_000598.2:n.541-471A>T
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