Canonical Allele Identifier: CA2259487718

Gene: CDC6

Linked Data

• dbSNP Id: rs2032735018

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40290326G>T , CM000679.2:g.40290326G>T	GRCh38
NC_000017.10:g.38446578G>T , CM000679.1:g.38446578G>T	GRCh37
NC_000017.9:g.35700104G>T	NCBI36
NG_028240.1:g.7433G>T
NG_028240.2:g.7448G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000209728.9:c.178+728G>T MANE Select	ENSP00000209728.4:n.178+728G>T
ENST00000649662.1:c.178+728G>T	ENSP00000497345.1:n.178+728G>T
ENST00000209728.8:c.178+728G>T	ENSP00000209728.4:n.178+728G>T
ENST00000473555.1:c.178+728G>T	ENSP00000464047.1:n.178+728G>T
ENST00000577249.1:c.178+728G>T	ENSP00000463004.1:n.178+728G>T
ENST00000580824.5:c.178+728G>T	ENSP00000463635.1:n.178+728G>T
NM_001254.3:c.178+728G>T	NP_001245.1:n.178+728G>T
XM_011525541.1:c.178+728G>T	XP_011523843.1:n.178+728G>T
XM_011525542.1:c.178+728G>T	XP_011523844.1:n.178+728G>T
NM_001254.4:c.178+728G>T MANE Select	NP_001245.1:n.178+728G>T
XM_011525541.2:c.178+728G>T	XP_011523843.1:n.178+728G>T