Canonical Allele Identifier: CA10586847

Gene: GATA2

Linked Data

• ClinVar Variation Id: 257568
• ClinVar RCV Id: RCV000253398
• dbSNP Id: rs886038417
• MyVariant Identifiers: chr3:g.128202853A>G (hg19) ; chr3:g.128484010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128484010A>G , CM000665.2:g.128484010A>G	GRCh38
NC_000003.11:g.128202853A>G , CM000665.1:g.128202853A>G	GRCh37
NC_000003.10:g.129685543A>G	NCBI36
NG_029334.1:g.14178T>C , LRG_295:g.14178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.872-5T>C MANE Plus Clinical	ENSP00000417074.1:n.872-5T>C
ENST00000696466.1:c.1154-5T>C	ENSP00000512647.1:n.1154-5T>C
ENST00000341105.7:c.872-5T>C MANE Select	ENSP00000345681.2:n.872-5T>C
ENST00000341105.6:c.872-5T>C	ENSP00000345681.2:n.872-5T>C
ENST00000430265.6:c.872-5T>C	ENSP00000400259.2:n.872-5T>C
ENST00000487848.5:c.872-5T>C	ENSP00000417074.1:n.872-5T>C
NM_001145661.1:c.872-5T>C , LRG_295t1:c.872-5T>C	NP_001139133.1:n.872-5T>C
NM_001145662.1:c.872-5T>C	NP_001139134.1:n.872-5T>C
NM_032638.4:c.872-5T>C , LRG_295t2:c.872-5T>C	NP_116027.2:n.872-5T>C
NM_001145661.2:c.872-5T>C MANE Plus Clinical	NP_001139133.1:n.872-5T>C
NM_032638.5:c.872-5T>C MANE Select	NP_116027.2:n.872-5T>C