Canonical Allele Identifier: CA622193901

Gene: ORC6

Linked Data

• dbSNP Id: rs1423050984
• gnomAD v2: 16-46727000-T-C
• gnomAD v4: 16-46693088-T-C
• MyVariant Identifiers: chr16:g.46727000T>C (hg19) ; chr16:g.46693088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.46693088T>C , CM000678.2:g.46693088T>C	GRCh38
NC_000016.9:g.46727000T>C , CM000678.1:g.46727000T>C	GRCh37
NC_000016.8:g.45284501T>C	NCBI36
NG_028241.1:g.8443T>C
NG_029970.1:g.1145A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000219097.7:c.360-5T>C MANE Select	ENSP00000219097.2:n.360-5T>C
ENST00000219097.6:c.360-5T>C	ENSP00000219097.2:n.360-5T>C
ENST00000563306.5:n.443-5T>C
ENST00000563599.5:c.*182-5T>C	ENSP00000454299.1:n.*182-5T>C
ENST00000566860.1:c.213-5T>C	ENSP00000456981.1:n.213-5T>C
ENST00000568364.6:c.360-5T>C	ENSP00000457282.2:n.360-5T>C
ENST00000569239.5:n.407-5T>C
ENST00000570260.2:n.359-5T>C
NM_014321.3:c.360-5T>C	NP_055136.1:n.360-5T>C
NR_037620.1:n.479-5T>C
XM_011522978.1:c.360-5T>C	XP_011521280.1:n.360-5T>C
XM_011522978.3:c.360-5T>C	XP_011521280.1:n.360-5T>C
NM_014321.4:c.360-5T>C MANE Select	NP_055136.1:n.360-5T>C
NR_037620.2:n.466-5T>C