Canonical Allele Identifier: CA10611359
Gene: ORC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 297590
ClinVar RCV Id: RCV000395639
dbSNP Id: rs886046401
gnomAD v3: 1-52404439-G-C
gnomAD v4: 1-52404439-G-C
MyVariant Identifiers: chr1:g.52870111G>C (hg19) chr1:g.52404439G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.52404439G>C , CM000663.2:g.52404439G>C GRCh38
NC_000001.10:g.52870111G>C , CM000663.1:g.52870111G>C GRCh37
NC_000001.9:g.52642699G>C NCBI36
NG_028251.1:g.5033C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371568.7:c.-199C>G ENSP00000360623.3:n.-199C>G
NM_001190818.1:c.-196C>G NP_001177747.1:n.-196C>G
NM_001190819.1:c.-199C>G NP_001177748.1:n.-199C>G
NM_004153.3:c.-199C>G NP_004144.2:n.-199C>G
XM_017001388.2:c.-199C>G XP_016856877.1:n.-199C>G
XM_017001389.2:c.-999C>G XP_016856878.1:n.-999C>G
Search 100 bp 5'
Search 100 bp 3'