Canonical Allele Identifier: CA2570985034
Gene: CDK6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92635062T>C , CM000669.2:g.92635062T>C GRCh38
NC_000007.13:g.92264376T>C , CM000669.1:g.92264376T>C GRCh37
NC_000007.12:g.92102312T>C NCBI36
NG_015888.1:g.206566A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000424848.3:c.648-11976A>G MANE Select ENSP00000397087.3:n.648-11976A>G
ENST00000265734.8:c.648-11976A>G ENSP00000265734.4:n.648-11976A>G
ENST00000424848.2:c.648-11976A>G ENSP00000397087.2:n.648-11976A>G
NM_001145306.1:c.648-11976A>G NP_001138778.1:n.648-11976A>G
NM_001259.6:c.648-11976A>G NP_001250.1:n.648-11976A>G
XM_006715835.1:c.648-11976A>G XP_006715898.1:n.648-11976A>G
XM_011515731.1:c.648-11976A>G XP_011514033.1:n.648-11976A>G
XR_927748.1:n.465-6897T>C
NM_001259.7:c.648-11976A>G NP_001250.1:n.648-11976A>G
XM_006715835.2:c.648-11976A>G XP_006715898.1:n.648-11976A>G
XR_002956577.1:n.7114A>G
XR_002956578.1:n.4762A>G
NM_001145306.2:c.648-11976A>G MANE Select NP_001138778.1:n.648-11976A>G
NM_001259.8:c.648-11976A>G NP_001250.1:n.648-11976A>G