Canonical Allele Identifier: CA113853

Gene: CDK9 MIR2861

Linked Data

• ClinVar Variation Id: 106
• ClinVar RCV Id: RCV000000126
• dbSNP Id: rs794728003
• gnomAD v3: 9-127785950-C-G
• gnomAD v4: 9-127785950-C-G
• MyVariant Identifiers: chr9:g.130548229C>G (hg19) ; chr9:g.127785950C>G (hg38)
• PubMed: PMID:19920351

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127785950C>G , CM000671.2:g.127785950C>G	GRCh38
NC_000009.11:g.130548229C>G , CM000671.1:g.130548229C>G	GRCh37
NC_000009.10:g.129588050C>G	NCBI36
NG_029812.1:g.5033C>G
NG_033942.1:g.4925C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421939.5:c.153C>G (CDK9)	ENSP00000395872.1:p.Leu51=
NR_036055.1:n.33C>G (MIR2861)
XR_002956743.1:n.413C>G (CDK9)