Canonical Allele Identifier: CA843873016

Gene: CDK6

Linked Data

• dbSNP Id: rs1375816661
• gnomAD v3: 7-92635159-T-A
• gnomAD v4: 7-92635159-T-A
• MyVariant Identifiers: chr7:g.92264473T>A (hg19) ; chr7:g.92635159T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635159T>A , CM000669.2:g.92635159T>A	GRCh38
NC_000007.13:g.92264473T>A , CM000669.1:g.92264473T>A	GRCh37
NC_000007.12:g.92102409T>A	NCBI36
NG_015888.1:g.206469A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.648-12073A>T MANE Select	ENSP00000397087.3:n.648-12073A>T
ENST00000265734.8:c.648-12073A>T	ENSP00000265734.4:n.648-12073A>T
ENST00000424848.2:c.648-12073A>T	ENSP00000397087.2:n.648-12073A>T
NM_001145306.1:c.648-12073A>T	NP_001138778.1:n.648-12073A>T
NM_001259.6:c.648-12073A>T	NP_001250.1:n.648-12073A>T
XM_006715835.1:c.648-12073A>T	XP_006715898.1:n.648-12073A>T
XM_011515731.1:c.648-12073A>T	XP_011514033.1:n.648-12073A>T
XR_927748.1:n.465-6800T>A
NM_001259.7:c.648-12073A>T	NP_001250.1:n.648-12073A>T
XM_006715835.2:c.648-12073A>T	XP_006715898.1:n.648-12073A>T
XR_002956577.1:n.7017A>T
XR_002956578.1:n.4665A>T
NM_001145306.2:c.648-12073A>T MANE Select	NP_001138778.1:n.648-12073A>T
NM_001259.8:c.648-12073A>T	NP_001250.1:n.648-12073A>T