Canonical Allele Identifier: CA12593141
Gene: CDK6 HGNC NCBI

Linked Data

dbSNP Id: rs42235
gnomAD v2: 7-92248076-C-T
gnomAD v3: 7-92618762-C-T
gnomAD v4: 7-92618762-C-T
MyVariant Identifiers: chr7:g.92248076C>T (hg19) chr7:g.92618762C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92618762C>T , CM000669.2:g.92618762C>T GRCh38
NC_000007.13:g.92248076C>T , CM000669.1:g.92248076C>T GRCh37
NC_000007.12:g.92086012C>T NCBI36
NG_015888.1:g.222866G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000424848.3:c.699-555G>A MANE Select ENSP00000397087.3:n.699-555G>A
ENST00000265734.8:c.699-555G>A ENSP00000265734.4:n.699-555G>A
ENST00000424848.2:c.699-555G>A ENSP00000397087.2:n.699-555G>A
NM_001145306.1:c.699-555G>A NP_001138778.1:n.699-555G>A
NM_001259.6:c.699-555G>A NP_001250.1:n.699-555G>A
XM_006715835.1:c.699-555G>A XP_006715898.1:n.699-555G>A
XM_011515731.1:c.699-555G>A XP_011514033.1:n.699-555G>A
NM_001259.7:c.699-555G>A NP_001250.1:n.699-555G>A
XM_006715835.2:c.699-555G>A XP_006715898.1:n.699-555G>A
NM_001145306.2:c.699-555G>A MANE Select NP_001138778.1:n.699-555G>A
NM_001259.8:c.699-555G>A NP_001250.1:n.699-555G>A
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