Canonical Allele Identifier: CA2633002480
Gene: ORC6 HGNC NCBI

Linked Data

gnomAD v4: 16-46698029-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698029C>A , CM000678.2:g.46698029C>A GRCh38
NC_000016.9:g.46731941C>A , CM000678.1:g.46731941C>A GRCh37
NC_000016.8:g.45289442C>A NCBI36
NG_028241.1:g.13384C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*444C>A MANE Select ENSP00000219097.2:n.*444C>A
ENST00000219097.6:c.*444C>A ENSP00000219097.2:n.*444C>A
ENST00000566860.1:c.*444C>A ENSP00000456981.1:n.*444C>A
ENST00000567000.2:n.1207C>A
NM_014321.3:c.*444C>A NP_055136.1:n.*444C>A
NR_037620.1:n.1322C>A
NM_014321.4:c.*444C>A MANE Select NP_055136.1:n.*444C>A
NR_037620.2:n.1309C>A
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