Canonical Allele Identifier: CA10639570

Gene: CDC6

Linked Data

• ClinVar Variation Id: 323052
• ClinVar RCV Id: RCV000322010
• dbSNP Id: rs886052901
• MyVariant Identifiers: chr17:g.38444350G>C (hg19) ; chr17:g.40288098G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40288098G>C , CM000679.2:g.40288098G>C	GRCh38
NC_000017.10:g.38444350G>C , CM000679.1:g.38444350G>C	GRCh37
NC_000017.9:g.35697876G>C	NCBI36
NG_028240.1:g.5205G>C
NG_028240.2:g.5220G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209728.9:c.-14+8G>C MANE Select	ENSP00000209728.4:n.-14+8G>C
ENST00000649662.1:c.-14+149G>C	ENSP00000497345.1:n.-14+149G>C
ENST00000209728.8:c.-14+8G>C	ENSP00000209728.4:n.-14+8G>C
ENST00000577249.1:c.-48G>C	ENSP00000463004.1:n.-48G>C
ENST00000580824.5:c.-14+61G>C	ENSP00000463635.1:n.-14+61G>C
NM_001254.3:c.-14+8G>C	NP_001245.1:n.-14+8G>C
XM_011525541.1:c.-14+8G>C	XP_011523843.1:n.-14+8G>C
XM_011525542.1:c.-48G>C	XP_011523844.1:n.-48G>C
NM_001254.4:c.-14+8G>C MANE Select	NP_001245.1:n.-14+8G>C
XM_011525541.2:c.-14+8G>C	XP_011523843.1:n.-14+8G>C