Canonical Allele Identifier: CA1104486189

Gene: CDK6

Linked Data

• dbSNP Id: rs1799267175
• gnomAD v3: 7-92754583-G-T
• gnomAD v4: 7-92754583-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92754583G>T , CM000669.2:g.92754583G>T	GRCh38
NC_000007.13:g.92383897G>T , CM000669.1:g.92383897G>T	GRCh37
NC_000007.12:g.92221833G>T	NCBI36
NG_015888.1:g.87045C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.369+20113C>A MANE Select	ENSP00000397087.3:n.369+20113C>A
ENST00000265734.8:c.369+20113C>A	ENSP00000265734.4:n.369+20113C>A
ENST00000424848.2:c.369+20113C>A	ENSP00000397087.2:n.369+20113C>A
NM_001145306.1:c.369+20113C>A	NP_001138778.1:n.369+20113C>A
NM_001259.6:c.369+20113C>A	NP_001250.1:n.369+20113C>A
XM_006715835.1:c.369+20113C>A	XP_006715898.1:n.369+20113C>A
XM_006715836.2:c.369+20113C>A	XP_006715899.1:n.369+20113C>A
XM_011515731.1:c.369+20113C>A	XP_011514033.1:n.369+20113C>A
NM_001259.7:c.369+20113C>A	NP_001250.1:n.369+20113C>A
XM_006715835.2:c.369+20113C>A	XP_006715898.1:n.369+20113C>A
NM_001145306.2:c.369+20113C>A MANE Select	NP_001138778.1:n.369+20113C>A
NM_001259.8:c.369+20113C>A	NP_001250.1:n.369+20113C>A