Canonical Allele Identifier: CA2220022623
Gene: ORC6 HGNC NCBI

Linked Data

dbSNP Id: rs1966542052

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698156G>C , CM000678.2:g.46698156G>C GRCh38
NC_000016.9:g.46732068G>C , CM000678.1:g.46732068G>C GRCh37
NC_000016.8:g.45289569G>C NCBI36
NG_028241.1:g.13511G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*571G>C MANE Select ENSP00000219097.2:n.*571G>C
ENST00000219097.6:c.*571G>C ENSP00000219097.2:n.*571G>C
ENST00000566860.1:c.*571G>C ENSP00000456981.1:n.*571G>C
ENST00000567000.2:n.1334G>C
NM_014321.3:c.*571G>C NP_055136.1:n.*571G>C
NR_037620.1:n.1449G>C
NM_014321.4:c.*571G>C MANE Select NP_055136.1:n.*571G>C
NR_037620.2:n.1436G>C