Canonical Allele Identifier: CA622179941
Gene: ORC6 HGNC NCBI

Linked Data

dbSNP Id: rs1166314612
gnomAD v2: 16-46732028-A-G
gnomAD v3: 16-46698116-A-G
gnomAD v4: 16-46698116-A-G
MyVariant Identifiers: chr16:g.46732028A>G (hg19) chr16:g.46698116A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698116A>G , CM000678.2:g.46698116A>G GRCh38
NC_000016.9:g.46732028A>G , CM000678.1:g.46732028A>G GRCh37
NC_000016.8:g.45289529A>G NCBI36
NG_028241.1:g.13471A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*531A>G MANE Select ENSP00000219097.2:n.*531A>G
ENST00000219097.6:c.*531A>G ENSP00000219097.2:n.*531A>G
ENST00000566860.1:c.*531A>G ENSP00000456981.1:n.*531A>G
ENST00000567000.2:n.1294A>G
NM_014321.3:c.*531A>G NP_055136.1:n.*531A>G
NR_037620.1:n.1409A>G
NM_014321.4:c.*531A>G MANE Select NP_055136.1:n.*531A>G
NR_037620.2:n.1396A>G
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