Canonical Allele Identifier: CA395817403
Community Standard Title: NM_014321.4(ORC6):c.2T>G (p.Met1Arg)
Gene: ORC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46689707T>G , CM000678.2:g.46689707T>G GRCh38
NC_000016.9:g.46723619T>G , CM000678.1:g.46723619T>G GRCh37
NC_000016.8:g.45281120T>G NCBI36
NG_028241.1:g.5062T>G
NG_029970.1:g.4526A>C

Transcript Alleles

HGVS Amino-acid Change
NM_014321.4:c.2T>G MANE Select NP_055136.1:p.Met1Arg
ENST00000219097.7:c.2T>G MANE Select ENSP00000219097.2:p.Met1Arg
NM_014321.3:c.2T>G NP_055136.1:p.Met1Arg
NR_037620.1:n.62T>G
NR_037620.2:n.49T>G
ENST00000219097.6:c.2T>G ENSP00000219097.2:p.Met1Arg
ENST00000563306.5:n.26T>G
ENST00000563599.5:c.2T>G ENSP00000454299.1:p.Met1Arg
ENST00000568364.6:c.2T>G ENSP00000457282.2:p.Met1Arg
ENST00000569239.5:n.49T>G
ENST00000570260.2:n.1T>G
XM_011522978.1:c.2T>G XP_011521280.1:p.Met1Arg
XM_011522978.3:c.2T>G XP_011521280.1:p.Met1Arg