Canonical Allele Identifier: CA2220022545
Gene: ORC6 HGNC NCBI

Linked Data

dbSNP Id: rs1966540361
gnomAD v4: 16-46698043-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698043A>G , CM000678.2:g.46698043A>G GRCh38
NC_000016.9:g.46731955A>G , CM000678.1:g.46731955A>G GRCh37
NC_000016.8:g.45289456A>G NCBI36
NG_028241.1:g.13398A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*458A>G MANE Select ENSP00000219097.2:n.*458A>G
ENST00000219097.6:c.*458A>G ENSP00000219097.2:n.*458A>G
ENST00000566860.1:c.*458A>G ENSP00000456981.1:n.*458A>G
ENST00000567000.2:n.1221A>G
NM_014321.3:c.*458A>G NP_055136.1:n.*458A>G
NR_037620.1:n.1336A>G
NM_014321.4:c.*458A>G MANE Select NP_055136.1:n.*458A>G
NR_037620.2:n.1323A>G
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