Canonical Allele Identifier: CA354412496

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1030046
• ClinVar RCV Id: RCV001331503
• dbSNP Id: rs2068620221
• MyVariant Identifiers: chr3:g.128199900G>A (hg19) ; chr3:g.128481057G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481057G>A , CM000665.2:g.128481057G>A	GRCh38
NC_000003.11:g.128199900G>A , CM000665.1:g.128199900G>A	GRCh37
NC_000003.10:g.129682590G>A	NCBI36
NG_029334.1:g.17131C>T , LRG_295:g.17131C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1405C>T MANE Plus Clinical	ENSP00000417074.1:p.His469Tyr
ENST00000696466.1:c.1687C>T	ENSP00000512647.1:p.His563Tyr
ENST00000696672.1:c.380C>T	ENSP00000512796.1:p.Pro127Leu
ENST00000341105.7:c.1405C>T MANE Select	ENSP00000345681.2:p.His469Tyr
ENST00000341105.6:c.1405C>T	ENSP00000345681.2:p.His469Tyr
ENST00000430265.6:c.1363C>T	ENSP00000400259.2:p.His455Tyr
ENST00000487848.5:c.1405C>T	ENSP00000417074.1:p.His469Tyr
ENST00000489987.1:n.522C>T
NM_001145661.1:c.1405C>T , LRG_295t1:c.1405C>T	NP_001139133.1:p.His469Tyr
NM_001145662.1:c.1363C>T	NP_001139134.1:p.His455Tyr
NM_032638.4:c.1405C>T , LRG_295t2:c.1405C>T	NP_116027.2:p.His469Tyr
NM_001145661.2:c.1405C>T MANE Plus Clinical	NP_001139133.1:p.His469Tyr
NM_032638.5:c.1405C>T MANE Select	NP_116027.2:p.His469Tyr