Canonical Allele Identifier: CA2633002358
Gene: ORC6 HGNC NCBI

Linked Data

gnomAD v4: 16-46697991-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46697991T>A , CM000678.2:g.46697991T>A GRCh38
NC_000016.9:g.46731903T>A , CM000678.1:g.46731903T>A GRCh37
NC_000016.8:g.45289404T>A NCBI36
NG_028241.1:g.13346T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*406T>A MANE Select ENSP00000219097.2:n.*406T>A
ENST00000219097.6:c.*406T>A ENSP00000219097.2:n.*406T>A
ENST00000566860.1:c.*406T>A ENSP00000456981.1:n.*406T>A
ENST00000567000.2:n.1169T>A
NM_014321.3:c.*406T>A NP_055136.1:n.*406T>A
NR_037620.1:n.1284T>A
NM_014321.4:c.*406T>A MANE Select NP_055136.1:n.*406T>A
NR_037620.2:n.1271T>A
Search 100 bp 5'
Search 100 bp 3'