Canonical Allele Identifier: CA625963491

Gene: CDC6

Linked Data

• dbSNP Id: rs1269679522
• gnomAD v2: 17-38446601-C-G
• gnomAD v3: 17-40290349-C-G
• gnomAD v4: 17-40290349-C-G
• MyVariant Identifiers: chr17:g.38446601C>G (hg19) ; chr17:g.40290349C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40290349C>G , CM000679.2:g.40290349C>G	GRCh38
NC_000017.10:g.38446601C>G , CM000679.1:g.38446601C>G	GRCh37
NC_000017.9:g.35700127C>G	NCBI36
NG_028240.1:g.7456C>G
NG_028240.2:g.7471C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000209728.9:c.179-709C>G MANE Select	ENSP00000209728.4:n.179-709C>G
ENST00000649662.1:c.179-709C>G	ENSP00000497345.1:n.179-709C>G
ENST00000209728.8:c.179-709C>G	ENSP00000209728.4:n.179-709C>G
ENST00000473555.1:c.179-709C>G	ENSP00000464047.1:n.179-709C>G
ENST00000577249.1:c.179-709C>G	ENSP00000463004.1:n.179-709C>G
ENST00000580824.5:c.179-709C>G	ENSP00000463635.1:n.179-709C>G
NM_001254.3:c.179-709C>G	NP_001245.1:n.179-709C>G
XM_011525541.1:c.179-709C>G	XP_011523843.1:n.179-709C>G
XM_011525542.1:c.179-709C>G	XP_011523844.1:n.179-709C>G
NM_001254.4:c.179-709C>G MANE Select	NP_001245.1:n.179-709C>G
XM_011525541.2:c.179-709C>G	XP_011523843.1:n.179-709C>G