Canonical Allele Identifier: CA456509781
Gene: CDK6 HGNC NCBI

Linked Data

dbSNP Id: rs2116603394
MyVariant Identifiers: chr7:g.92300844G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92671530G>A , CM000669.2:g.92671530G>A GRCh38
NC_000007.13:g.92300844G>A , CM000669.1:g.92300844G>A GRCh37
NC_000007.12:g.92138780G>A NCBI36
NG_015888.1:g.170098C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000424848.3:c.543C>T MANE Select ENSP00000397087.3:p.Val181=
ENST00000265734.8:c.543C>T ENSP00000265734.4:p.Val181=
ENST00000424848.2:c.543C>T ENSP00000397087.2:p.Val181=
ENST00000473078.1:n.91C>T
NM_001145306.1:c.543C>T NP_001138778.1:p.Val181=
NM_001259.6:c.543C>T NP_001250.1:p.Val181=
XM_006715835.1:c.543C>T XP_006715898.1:p.Val181=
XM_011515731.1:c.543C>T XP_011514033.1:p.Val181=
NM_001259.7:c.543C>T NP_001250.1:p.Val181=
XM_006715835.2:c.543C>T XP_006715898.1:p.Val181=
NM_001145306.2:c.543C>T MANE Select NP_001138778.1:p.Val181=
NM_001259.8:c.543C>T NP_001250.1:p.Val181=