Canonical Allele Identifier: CA1873789228
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs1588923288

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325824A>C , CM000671.2:g.114325824A>C GRCh38
NC_000009.11:g.117088104A>C , CM000671.1:g.117088104A>C GRCh37
NC_000009.10:g.116127925A>C NCBI36
NG_012108.1:g.7802A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-468A>C MANE Select ENSP00000259396.8:n.541-468A>C
ENST00000259396.8:c.541-468A>C ENSP00000259396.8:n.541-468A>C
NM_000607.2:c.541-468A>C NP_000598.2:n.541-468A>C
NM_000607.3:c.541-468A>C NP_000598.2:n.541-468A>C
NM_000607.4:c.541-468A>C MANE Select NP_000598.2:n.541-468A>C