Canonical Allele Identifier: CA1873789203
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs2932682

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325796T>G , CM000671.2:g.114325796T>G GRCh38
NC_000009.11:g.117088076T>G , CM000671.1:g.117088076T>G GRCh37
NC_000009.10:g.116127897T>G NCBI36
NG_012108.1:g.7774T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-496T>G MANE Select ENSP00000259396.8:n.541-496T>G
ENST00000259396.8:c.541-496T>G ENSP00000259396.8:n.541-496T>G
NM_000607.2:c.541-496T>G NP_000598.2:n.541-496T>G
NM_000607.3:c.541-496T>G NP_000598.2:n.541-496T>G
NM_000607.4:c.541-496T>G MANE Select NP_000598.2:n.541-496T>G