Canonical Allele Identifier: CA1873789225
Gene: ORM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325823T= , CM000671.2:g.114325823T= GRCh38
NC_000009.11:g.117088103T= , CM000671.1:g.117088103T= GRCh37
NC_000009.10:g.116127924T= NCBI36
NG_012108.1:g.7801T=

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-469T= MANE Select ENSP00000259396.8:n.541-469T=
ENST00000259396.8:c.541-469T= ENSP00000259396.8:n.541-469T=
NM_000607.2:c.541-469T= NP_000598.2:n.541-469T=
NM_000607.3:c.541-469T= NP_000598.2:n.541-469T=
NM_000607.4:c.541-469T= MANE Select NP_000598.2:n.541-469T=
Search 100 bp 5'
Search 100 bp 3'