Canonical Allele Identifier: CA843873019

Gene: CDK6

Linked Data

• dbSNP Id: rs1298896243
• MyVariant Identifiers: chr7:g.92264475G>A (hg19) ; chr7:g.92635161G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92635161G>A , CM000669.2:g.92635161G>A	GRCh38
NC_000007.13:g.92264475G>A , CM000669.1:g.92264475G>A	GRCh37
NC_000007.12:g.92102411G>A	NCBI36
NG_015888.1:g.206467C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.648-12075C>T MANE Select	ENSP00000397087.3:n.648-12075C>T
ENST00000265734.8:c.648-12075C>T	ENSP00000265734.4:n.648-12075C>T
ENST00000424848.2:c.648-12075C>T	ENSP00000397087.2:n.648-12075C>T
NM_001145306.1:c.648-12075C>T	NP_001138778.1:n.648-12075C>T
NM_001259.6:c.648-12075C>T	NP_001250.1:n.648-12075C>T
XM_006715835.1:c.648-12075C>T	XP_006715898.1:n.648-12075C>T
XM_011515731.1:c.648-12075C>T	XP_011514033.1:n.648-12075C>T
XR_927748.1:n.465-6798G>A
NM_001259.7:c.648-12075C>T	NP_001250.1:n.648-12075C>T
XM_006715835.2:c.648-12075C>T	XP_006715898.1:n.648-12075C>T
XR_002956577.1:n.7015C>T
XR_002956578.1:n.4663C>T
NM_001145306.2:c.648-12075C>T MANE Select	NP_001138778.1:n.648-12075C>T
NM_001259.8:c.648-12075C>T	NP_001250.1:n.648-12075C>T