Canonical Allele Identifier: CA1104486197

Gene: CDK6

Linked Data

• dbSNP Id: rs1799267807
• gnomAD v3: 7-92754609-G-A
• gnomAD v4: 7-92754609-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92754609G>A , CM000669.2:g.92754609G>A	GRCh38
NC_000007.13:g.92383923G>A , CM000669.1:g.92383923G>A	GRCh37
NC_000007.12:g.92221859G>A	NCBI36
NG_015888.1:g.87019C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.369+20087C>T MANE Select	ENSP00000397087.3:n.369+20087C>T
ENST00000265734.8:c.369+20087C>T	ENSP00000265734.4:n.369+20087C>T
ENST00000424848.2:c.369+20087C>T	ENSP00000397087.2:n.369+20087C>T
NM_001145306.1:c.369+20087C>T	NP_001138778.1:n.369+20087C>T
NM_001259.6:c.369+20087C>T	NP_001250.1:n.369+20087C>T
XM_006715835.1:c.369+20087C>T	XP_006715898.1:n.369+20087C>T
XM_006715836.2:c.369+20087C>T	XP_006715899.1:n.369+20087C>T
XM_011515731.1:c.369+20087C>T	XP_011514033.1:n.369+20087C>T
NM_001259.7:c.369+20087C>T	NP_001250.1:n.369+20087C>T
XM_006715835.2:c.369+20087C>T	XP_006715898.1:n.369+20087C>T
NM_001145306.2:c.369+20087C>T MANE Select	NP_001138778.1:n.369+20087C>T
NM_001259.8:c.369+20087C>T	NP_001250.1:n.369+20087C>T