Canonical Allele Identifier: CA161978380

Gene: CDK6

Linked Data

• dbSNP Id: rs975350406
• gnomAD v2: 7-92264341-C-T
• gnomAD v3: 7-92635027-C-T
• gnomAD v4: 7-92635027-C-T
• MyVariant Identifiers: chr7:g.92264341C>T (hg19) ; chr7:g.92635027C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635027C>T , CM000669.2:g.92635027C>T	GRCh38
NC_000007.13:g.92264341C>T , CM000669.1:g.92264341C>T	GRCh37
NC_000007.12:g.92102277C>T	NCBI36
NG_015888.1:g.206601G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.648-11941G>A MANE Select	ENSP00000397087.3:n.648-11941G>A
ENST00000265734.8:c.648-11941G>A	ENSP00000265734.4:n.648-11941G>A
ENST00000424848.2:c.648-11941G>A	ENSP00000397087.2:n.648-11941G>A
NM_001145306.1:c.648-11941G>A	NP_001138778.1:n.648-11941G>A
NM_001259.6:c.648-11941G>A	NP_001250.1:n.648-11941G>A
XM_006715835.1:c.648-11941G>A	XP_006715898.1:n.648-11941G>A
XM_011515731.1:c.648-11941G>A	XP_011514033.1:n.648-11941G>A
XR_927748.1:n.465-6932C>T
NM_001259.7:c.648-11941G>A	NP_001250.1:n.648-11941G>A
XM_006715835.2:c.648-11941G>A	XP_006715898.1:n.648-11941G>A
XR_002956577.1:n.7149G>A
XR_002956578.1:n.4797G>A
NM_001145306.2:c.648-11941G>A MANE Select	NP_001138778.1:n.648-11941G>A
NM_001259.8:c.648-11941G>A	NP_001250.1:n.648-11941G>A