Canonical Allele Identifier: CA576497625

Gene: CDK6

Linked Data

• dbSNP Id: rs1489758477
• gnomAD v2: 7-92246967-G-T
• gnomAD v3: 7-92617653-G-T
• gnomAD v4: 7-92617653-G-T
• MyVariant Identifiers: chr7:g.92246967G>T (hg19) ; chr7:g.92617653G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92617653G>T , CM000669.2:g.92617653G>T	GRCh38
NC_000007.13:g.92246967G>T , CM000669.1:g.92246967G>T	GRCh37
NC_000007.12:g.92084903G>T	NCBI36
NG_015888.1:g.223975C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424848.3:c.834+419C>A MANE Select	ENSP00000397087.3:n.834+419C>A
ENST00000265734.8:c.834+419C>A	ENSP00000265734.4:n.834+419C>A
ENST00000424848.2:c.834+419C>A	ENSP00000397087.2:n.834+419C>A
ENST00000467166.1:n.206+419C>A
NM_001145306.1:c.834+419C>A	NP_001138778.1:n.834+419C>A
NM_001259.6:c.834+419C>A	NP_001250.1:n.834+419C>A
XM_006715835.1:c.834+419C>A	XP_006715898.1:n.834+419C>A
XM_011515731.1:c.834+419C>A	XP_011514033.1:n.834+419C>A
NM_001259.7:c.834+419C>A	NP_001250.1:n.834+419C>A
XM_006715835.2:c.834+419C>A	XP_006715898.1:n.834+419C>A
NM_001145306.2:c.834+419C>A MANE Select	NP_001138778.1:n.834+419C>A
NM_001259.8:c.834+419C>A	NP_001250.1:n.834+419C>A