Canonical Allele Identifier: CA162099216

Gene: CDK6

Linked Data

• dbSNP Id: rs775366809
• gnomAD v3: 7-92754646-C-G
• gnomAD v4: 7-92754646-C-G
• MyVariant Identifiers: chr7:g.92383960C>G (hg19) ; chr7:g.92754646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92754646C>G , CM000669.2:g.92754646C>G	GRCh38
NC_000007.13:g.92383960C>G , CM000669.1:g.92383960C>G	GRCh37
NC_000007.12:g.92221896C>G	NCBI36
NG_015888.1:g.86982G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.369+20050G>C MANE Select	ENSP00000397087.3:n.369+20050G>C
ENST00000265734.8:c.369+20050G>C	ENSP00000265734.4:n.369+20050G>C
ENST00000424848.2:c.369+20050G>C	ENSP00000397087.2:n.369+20050G>C
NM_001145306.1:c.369+20050G>C	NP_001138778.1:n.369+20050G>C
NM_001259.6:c.369+20050G>C	NP_001250.1:n.369+20050G>C
XM_006715835.1:c.369+20050G>C	XP_006715898.1:n.369+20050G>C
XM_006715836.2:c.369+20050G>C	XP_006715899.1:n.369+20050G>C
XM_011515731.1:c.369+20050G>C	XP_011514033.1:n.369+20050G>C
NM_001259.7:c.369+20050G>C	NP_001250.1:n.369+20050G>C
XM_006715835.2:c.369+20050G>C	XP_006715898.1:n.369+20050G>C
NM_001145306.2:c.369+20050G>C MANE Select	NP_001138778.1:n.369+20050G>C
NM_001259.8:c.369+20050G>C	NP_001250.1:n.369+20050G>C