Canonical Allele Identifier: CA1873789202
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1829759658
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325791T>A , CM000671.2:g.114325791T>A GRCh38
NC_000009.11:g.117088071T>A , CM000671.1:g.117088071T>A GRCh37
NC_000009.10:g.116127892T>A NCBI36
NG_012108.1:g.7769T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-501T>A MANE Select ENSP00000259396.8:n.541-501T>A
ENST00000259396.8:c.541-501T>A ENSP00000259396.8:n.541-501T>A
NM_000607.2:c.541-501T>A NP_000598.2:n.541-501T>A
NM_000607.3:c.541-501T>A NP_000598.2:n.541-501T>A
NM_000607.4:c.541-501T>A MANE Select NP_000598.2:n.541-501T>A
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