Canonical Allele Identifier: CA15486940
Gene: CDK6 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.92607515A>G
GRCh37 chr7:g.92236829A>G
gnomAD v2:
7:92236829 A / G
gnomAD v3:
7:92607515 A / G
gnomAD v4:
chr7-92607515-A-G
Joint Max Group AF 0.21308902 (NFE)
Genomes Max Group AF 0.21399864 (NFE)
Exomes Max Group AF 0.20970669 (NFE)
dbSNP:
4272
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92607515A>G , CM000669.2:g.92607515A>G GRCh38
NC_000007.13:g.92236829A>G , CM000669.1:g.92236829A>G GRCh37
NC_000007.12:g.92074765A>G NCBI36
NG_015888.1:g.234113T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.*7625T>C MANE Select ENSP00000397087.3:n.*7625T>C
ENST00000265734.8:c.*7625T>C ENSP00000265734.4:n.*7625T>C
NM_001145306.1:c.*7625T>C NP_001138778.1:n.*7625T>C
NM_001259.6:c.*7625T>C NP_001250.1:n.*7625T>C
XM_006715835.1:c.*7625T>C XP_006715898.1:n.*7625T>C
XM_011515731.1:c.*7625T>C XP_011514033.1:n.*7625T>C
NM_001259.7:c.*7625T>C NP_001250.1:n.*7625T>C
XM_006715835.2:c.*7625T>C XP_006715898.1:n.*7625T>C
NM_001145306.2:c.*7625T>C MANE Select NP_001138778.1:n.*7625T>C
NM_001259.8:c.*7625T>C NP_001250.1:n.*7625T>C
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