Canonical Allele Identifier: CA2220022597
Gene: ORC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46698117A= , CM000678.2:g.46698117A= GRCh38
NC_000016.9:g.46732029A= , CM000678.1:g.46732029A= GRCh37
NC_000016.8:g.45289530A= NCBI36
NG_028241.1:g.13472A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*532A= MANE Select ENSP00000219097.2:n.*532A=
ENST00000219097.6:c.*532A= ENSP00000219097.2:n.*532A=
ENST00000566860.1:c.*532A= ENSP00000456981.1:n.*532A=
ENST00000567000.2:n.1295A=
NM_014321.3:c.*532A= NP_055136.1:n.*532A=
NR_037620.1:n.1410A=
NM_014321.4:c.*532A= MANE Select NP_055136.1:n.*532A=
NR_037620.2:n.1397A=