Canonical Allele Identifier: CA395819177

Gene: ORC6

Linked Data

• MyVariant Identifiers: chr16:g.46727009G>C (hg19) ; chr16:g.46693097G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46693097G>C , CM000678.2:g.46693097G>C	GRCh38
NC_000016.9:g.46727009G>C , CM000678.1:g.46727009G>C	GRCh37
NC_000016.8:g.45284510G>C	NCBI36
NG_028241.1:g.8452G>C
NG_029970.1:g.1136C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000219097.7:c.364G>C MANE Select	ENSP00000219097.2:p.Glu122Gln
ENST00000219097.6:c.364G>C	ENSP00000219097.2:p.Glu122Gln
ENST00000563306.5:n.447G>C
ENST00000563599.5:c.*186G>C	ENSP00000454299.1:n.*186G>C
ENST00000566860.1:c.217G>C	ENSP00000456981.1:p.Glu73Gln
ENST00000568364.6:c.364G>C	ENSP00000457282.2:p.Glu122Gln
ENST00000569239.5:n.411G>C
ENST00000570260.2:n.363G>C
NM_014321.3:c.364G>C	NP_055136.1:p.Glu122Gln
NR_037620.1:n.483G>C
XM_011522978.1:c.364G>C	XP_011521280.1:p.Glu122Gln
XM_011522978.3:c.364G>C	XP_011521280.1:p.Glu122Gln
NM_014321.4:c.364G>C MANE Select	NP_055136.1:p.Glu122Gln
NR_037620.2:n.470G>C