Canonical Allele Identifier: CA12674195
Gene: CDK6 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.92779056C>T
GRCh37 chr7:g.92408370C>T
gnomAD v2:
7:92408370 C / T
gnomAD v3:
7:92779056 C / T
gnomAD v4:
chr7-92779056-C-T
Joint Max Group AF 0.33162821 (EAS)
Genomes Max Group AF 0.33162821 (EAS)
dbSNP:
445
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92779056C>T , CM000669.2:g.92779056C>T GRCh38
NC_000007.13:g.92408370C>T , CM000669.1:g.92408370C>T GRCh37
NC_000007.12:g.92246306C>T NCBI36
NG_015888.1:g.62572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.234-4225G>A MANE Select ENSP00000397087.3:n.234-4225G>A
ENST00000265734.8:c.234-4225G>A ENSP00000265734.4:n.234-4225G>A
ENST00000424848.2:c.234-4225G>A ENSP00000397087.2:n.234-4225G>A
NM_001145306.1:c.234-4225G>A NP_001138778.1:n.234-4225G>A
NM_001259.6:c.234-4225G>A NP_001250.1:n.234-4225G>A
XM_006715835.1:c.234-4225G>A XP_006715898.1:n.234-4225G>A
XM_006715836.2:c.234-4225G>A XP_006715899.1:n.234-4225G>A
XM_011515731.1:c.234-4225G>A XP_011514033.1:n.234-4225G>A
NM_001259.7:c.234-4225G>A NP_001250.1:n.234-4225G>A
XM_006715835.2:c.234-4225G>A XP_006715898.1:n.234-4225G>A
NM_001145306.2:c.234-4225G>A MANE Select NP_001138778.1:n.234-4225G>A
NM_001259.8:c.234-4225G>A NP_001250.1:n.234-4225G>A
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