Canonical Allele Identifier: CA858953520
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1460572735
MyVariant Identifiers: chr9:g.117088097G>A (hg19) chr9:g.114325817G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325817G>A , CM000671.2:g.114325817G>A GRCh38
NC_000009.11:g.117088097G>A , CM000671.1:g.117088097G>A GRCh37
NC_000009.10:g.116127918G>A NCBI36
NG_012108.1:g.7795G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-475G>A MANE Select ENSP00000259396.8:n.541-475G>A
ENST00000259396.8:c.541-475G>A ENSP00000259396.8:n.541-475G>A
NM_000607.2:c.541-475G>A NP_000598.2:n.541-475G>A
NM_000607.3:c.541-475G>A NP_000598.2:n.541-475G>A
NM_000607.4:c.541-475G>A MANE Select NP_000598.2:n.541-475G>A
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