Canonical Allele Identifier: CA1104506226

Gene: CDK6

Linked Data

• dbSNP Id: rs1796137239
• gnomAD v3: 7-92635006-A-C
• gnomAD v4: 7-92635006-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635006A>C , CM000669.2:g.92635006A>C	GRCh38
NC_000007.13:g.92264320A>C , CM000669.1:g.92264320A>C	GRCh37
NC_000007.12:g.92102256A>C	NCBI36
NG_015888.1:g.206622T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.648-11920T>G MANE Select	ENSP00000397087.3:n.648-11920T>G
ENST00000265734.8:c.648-11920T>G	ENSP00000265734.4:n.648-11920T>G
ENST00000424848.2:c.648-11920T>G	ENSP00000397087.2:n.648-11920T>G
NM_001145306.1:c.648-11920T>G	NP_001138778.1:n.648-11920T>G
NM_001259.6:c.648-11920T>G	NP_001250.1:n.648-11920T>G
XM_006715835.1:c.648-11920T>G	XP_006715898.1:n.648-11920T>G
XM_011515731.1:c.648-11920T>G	XP_011514033.1:n.648-11920T>G
XR_927748.1:n.465-6953A>C
NM_001259.7:c.648-11920T>G	NP_001250.1:n.648-11920T>G
XM_006715835.2:c.648-11920T>G	XP_006715898.1:n.648-11920T>G
XR_002956577.1:n.7170T>G
XR_002956578.1:n.4818T>G
NM_001145306.2:c.648-11920T>G MANE Select	NP_001138778.1:n.648-11920T>G
NM_001259.8:c.648-11920T>G	NP_001250.1:n.648-11920T>G