Canonical Allele Identifier: CA10650065
Gene: CDC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 323064
ClinVar RCV Id: RCV000359109
dbSNP Id: rs575274633
gnomAD v2: 17-38458611-G-T
gnomAD v3: 17-40302359-G-T
gnomAD v4: 17-40302359-G-T
MyVariant Identifiers: chr17:g.38458611G>T (hg19) chr17:g.40302359G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40302359G>T , CM000679.2:g.40302359G>T GRCh38
NC_000017.10:g.38458611G>T , CM000679.1:g.38458611G>T GRCh37
NC_000017.9:g.35712137G>T NCBI36
NG_028240.1:g.19466G>T
NG_028240.2:g.19481G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000209728.9:c.*358G>T MANE Select ENSP00000209728.4:n.*358G>T
ENST00000209728.8:c.*358G>T ENSP00000209728.4:n.*358G>T
NM_001254.3:c.*358G>T NP_001245.1:n.*358G>T
XM_011525541.1:c.*358G>T XP_011523843.1:n.*358G>T
XM_011525542.1:c.*358G>T XP_011523844.1:n.*358G>T
NM_001254.4:c.*358G>T MANE Select NP_001245.1:n.*358G>T
XM_011525541.2:c.*358G>T XP_011523843.1:n.*358G>T
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