Canonical Allele Identifier: CA1873789206
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1829759801
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325797C>A , CM000671.2:g.114325797C>A GRCh38
NC_000009.11:g.117088077C>A , CM000671.1:g.117088077C>A GRCh37
NC_000009.10:g.116127898C>A NCBI36
NG_012108.1:g.7775C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-495C>A MANE Select ENSP00000259396.8:n.541-495C>A
ENST00000259396.8:c.541-495C>A ENSP00000259396.8:n.541-495C>A
NM_000607.2:c.541-495C>A NP_000598.2:n.541-495C>A
NM_000607.3:c.541-495C>A NP_000598.2:n.541-495C>A
NM_000607.4:c.541-495C>A MANE Select NP_000598.2:n.541-495C>A
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