Canonical Allele Identifier: CA10639574
Gene: CDC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 323061
ClinVar RCV Id: RCV000359823
dbSNP Id: rs141386457
gnomAD v2: 17-38458434-A-G
gnomAD v3: 17-40302182-A-G
gnomAD v4: 17-40302182-A-G
MyVariant Identifiers: chr17:g.38458434A>G (hg19) chr17:g.40302182A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40302182A>G , CM000679.2:g.40302182A>G GRCh38
NC_000017.10:g.38458434A>G , CM000679.1:g.38458434A>G GRCh37
NC_000017.9:g.35711960A>G NCBI36
NG_028240.1:g.19289A>G
NG_028240.2:g.19304A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000209728.9:c.*181A>G MANE Select ENSP00000209728.4:n.*181A>G
ENST00000649662.1:c.*181A>G ENSP00000497345.1:n.*181A>G
ENST00000209728.8:c.*181A>G ENSP00000209728.4:n.*181A>G
NM_001254.3:c.*181A>G NP_001245.1:n.*181A>G
XM_011525541.1:c.*181A>G XP_011523843.1:n.*181A>G
XM_011525542.1:c.*181A>G XP_011523844.1:n.*181A>G
NM_001254.4:c.*181A>G MANE Select NP_001245.1:n.*181A>G
XM_011525541.2:c.*181A>G XP_011523843.1:n.*181A>G
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