Canonical Allele Identifier: CA2580895847
Gene: ORM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325784T>G , CM000671.2:g.114325784T>G GRCh38
NC_000009.11:g.117088064T>G , CM000671.1:g.117088064T>G GRCh37
NC_000009.10:g.116127885T>G NCBI36
NG_012108.1:g.7762T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-508T>G MANE Select ENSP00000259396.8:n.541-508T>G
ENST00000259396.8:c.541-508T>G ENSP00000259396.8:n.541-508T>G
NM_000607.2:c.541-508T>G NP_000598.2:n.541-508T>G
NM_000607.3:c.541-508T>G NP_000598.2:n.541-508T>G
NM_000607.4:c.541-508T>G MANE Select NP_000598.2:n.541-508T>G
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