Canonical Allele Identifier: CA161978407

Gene: CDK6

Linked Data

• dbSNP Id: rs563436429
• gnomAD v2: 7-92264394-A-G
• gnomAD v3: 7-92635080-A-G
• gnomAD v4: 7-92635080-A-G
• MyVariant Identifiers: chr7:g.92264394A>G (hg19) ; chr7:g.92635080A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635080A>G , CM000669.2:g.92635080A>G	GRCh38
NC_000007.13:g.92264394A>G , CM000669.1:g.92264394A>G	GRCh37
NC_000007.12:g.92102330A>G	NCBI36
NG_015888.1:g.206548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.648-11994T>C MANE Select	ENSP00000397087.3:n.648-11994T>C
ENST00000265734.8:c.648-11994T>C	ENSP00000265734.4:n.648-11994T>C
ENST00000424848.2:c.648-11994T>C	ENSP00000397087.2:n.648-11994T>C
NM_001145306.1:c.648-11994T>C	NP_001138778.1:n.648-11994T>C
NM_001259.6:c.648-11994T>C	NP_001250.1:n.648-11994T>C
XM_006715835.1:c.648-11994T>C	XP_006715898.1:n.648-11994T>C
XM_011515731.1:c.648-11994T>C	XP_011514033.1:n.648-11994T>C
XR_927748.1:n.465-6879A>G
NM_001259.7:c.648-11994T>C	NP_001250.1:n.648-11994T>C
XM_006715835.2:c.648-11994T>C	XP_006715898.1:n.648-11994T>C
XR_002956577.1:n.7096T>C
XR_002956578.1:n.4744T>C
NM_001145306.2:c.648-11994T>C MANE Select	NP_001138778.1:n.648-11994T>C
NM_001259.8:c.648-11994T>C	NP_001250.1:n.648-11994T>C