Canonical Allele Identifier: CA368385463

Gene: CDK6

Linked Data

• dbSNP Id: rs606231255
• gnomAD v4: 7-92671484-C-A
• MyVariant Identifiers: chr7:g.92300798C>A (hg19) ; chr7:g.92671484C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92671484C>A , CM000669.2:g.92671484C>A	GRCh38
NC_000007.13:g.92300798C>A , CM000669.1:g.92300798C>A	GRCh37
NC_000007.12:g.92138734C>A	NCBI36
NG_015888.1:g.170144G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000424848.3:c.589G>T MANE Select	ENSP00000397087.3:p.Ala197Ser
ENST00000265734.8:c.589G>T	ENSP00000265734.4:p.Ala197Ser
ENST00000424848.2:c.589G>T	ENSP00000397087.2:p.Ala197Ser
ENST00000473078.1:n.137G>T
NM_001145306.1:c.589G>T	NP_001138778.1:p.Ala197Ser
NM_001259.6:c.589G>T	NP_001250.1:p.Ala197Ser
XM_006715835.1:c.589G>T	XP_006715898.1:p.Ala197Ser
XM_011515731.1:c.589G>T	XP_011514033.1:p.Ala197Ser
NM_001259.7:c.589G>T	NP_001250.1:p.Ala197Ser
XM_006715835.2:c.589G>T	XP_006715898.1:p.Ala197Ser
NM_001145306.2:c.589G>T MANE Select	NP_001138778.1:p.Ala197Ser
NM_001259.8:c.589G>T	NP_001250.1:p.Ala197Ser