Canonical Allele Identifier: CA2220022500
Gene: ORC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46697964A= , CM000678.2:g.46697964A= GRCh38
NC_000016.9:g.46731876A= , CM000678.1:g.46731876A= GRCh37
NC_000016.8:g.45289377A= NCBI36
NG_028241.1:g.13319A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219097.7:c.*379A= MANE Select ENSP00000219097.2:n.*379A=
ENST00000219097.6:c.*379A= ENSP00000219097.2:n.*379A=
ENST00000566860.1:c.*379A= ENSP00000456981.1:n.*379A=
ENST00000567000.2:n.1142A=
NM_014321.3:c.*379A= NP_055136.1:n.*379A=
NR_037620.1:n.1257A=
NM_014321.4:c.*379A= MANE Select NP_055136.1:n.*379A=
NR_037620.2:n.1244A=