Canonical Allele Identifier: CA12968703
Gene: ORM1 HGNC NCBI

Linked Data

dbSNP Id: rs2932682
gnomAD v2: 9-117088076-T-C
gnomAD v3: 9-114325796-T-C
gnomAD v4: 9-114325796-T-C
MyVariant Identifiers: chr9:g.117088076T>C (hg19) chr9:g.114325796T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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