Canonical Allele Identifier: CA290494631

Gene: CDC6

Linked Data

• dbSNP Id: rs1056418114
• gnomAD v3: 17-40290256-A-C
• gnomAD v4: 17-40290256-A-C
• MyVariant Identifiers: chr17:g.38446508A>C (hg19) ; chr17:g.40290256A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40290256A>C , CM000679.2:g.40290256A>C	GRCh38
NC_000017.10:g.38446508A>C , CM000679.1:g.38446508A>C	GRCh37
NC_000017.9:g.35700034A>C	NCBI36
NG_028240.1:g.7363A>C
NG_028240.2:g.7378A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000209728.9:c.178+658A>C MANE Select	ENSP00000209728.4:n.178+658A>C
ENST00000649662.1:c.178+658A>C	ENSP00000497345.1:n.178+658A>C
ENST00000209728.8:c.178+658A>C	ENSP00000209728.4:n.178+658A>C
ENST00000473555.1:c.178+658A>C	ENSP00000464047.1:n.178+658A>C
ENST00000577249.1:c.178+658A>C	ENSP00000463004.1:n.178+658A>C
ENST00000580824.5:c.178+658A>C	ENSP00000463635.1:n.178+658A>C
NM_001254.3:c.178+658A>C	NP_001245.1:n.178+658A>C
XM_011525541.1:c.178+658A>C	XP_011523843.1:n.178+658A>C
XM_011525542.1:c.178+658A>C	XP_011523844.1:n.178+658A>C
NM_001254.4:c.178+658A>C MANE Select	NP_001245.1:n.178+658A>C
XM_011525541.2:c.178+658A>C	XP_011523843.1:n.178+658A>C