Canonical Allele Identifier: CA15526881

Gene: CDK6

Linked Data

• dbSNP Id: rs10
• gnomAD v2: 7-92383888-A-C
• gnomAD v3: 7-92754574-A-C
• gnomAD v4: 7-92754574-A-C
• MyVariant Identifiers: chr7:g.92383888A>C (hg19) ; chr7:g.92754574A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92754574A>C , CM000669.2:g.92754574A>C	GRCh38
NC_000007.13:g.92383888A>C , CM000669.1:g.92383888A>C	GRCh37
NC_000007.12:g.92221824A>C	NCBI36
NG_015888.1:g.87054T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.369+20122T>G MANE Select	ENSP00000397087.3:n.369+20122T>G
ENST00000265734.8:c.369+20122T>G	ENSP00000265734.4:n.369+20122T>G
ENST00000424848.2:c.369+20122T>G	ENSP00000397087.2:n.369+20122T>G
NM_001145306.1:c.369+20122T>G	NP_001138778.1:n.369+20122T>G
NM_001259.6:c.369+20122T>G	NP_001250.1:n.369+20122T>G
XM_006715835.1:c.369+20122T>G	XP_006715898.1:n.369+20122T>G
XM_006715836.2:c.369+20122T>G	XP_006715899.1:n.369+20122T>G
XM_011515731.1:c.369+20122T>G	XP_011514033.1:n.369+20122T>G
NM_001259.7:c.369+20122T>G	NP_001250.1:n.369+20122T>G
XM_006715835.2:c.369+20122T>G	XP_006715898.1:n.369+20122T>G
NM_001145306.2:c.369+20122T>G MANE Select	NP_001138778.1:n.369+20122T>G
NM_001259.8:c.369+20122T>G	NP_001250.1:n.369+20122T>G