Canonical Allele Identifier: CA354406457

Gene: GATA2

Linked Data

• ClinVar Variation Id: 649115
• ClinVar RCV Id: RCV000803972
• dbSNP Id: rs1576748685
• MyVariant Identifiers: chr3:g.128204849C>T (hg19) ; chr3:g.128486006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128486006C>T , CM000665.2:g.128486006C>T	GRCh38
NC_000003.11:g.128204849C>T , CM000665.1:g.128204849C>T	GRCh37
NC_000003.10:g.129687539C>T	NCBI36
NG_029334.1:g.12182G>A , LRG_295:g.12182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.592G>A MANE Plus Clinical	ENSP00000417074.1:p.Ala198Thr
ENST00000696466.1:c.874G>A	ENSP00000512647.1:p.Ala292Thr
ENST00000341105.7:c.592G>A MANE Select	ENSP00000345681.2:p.Ala198Thr
ENST00000341105.6:c.592G>A	ENSP00000345681.2:p.Ala198Thr
ENST00000430265.6:c.592G>A	ENSP00000400259.2:p.Ala198Thr
ENST00000487848.5:c.592G>A	ENSP00000417074.1:p.Ala198Thr
NM_001145661.1:c.592G>A , LRG_295t1:c.592G>A	NP_001139133.1:p.Ala198Thr
NM_001145662.1:c.592G>A	NP_001139134.1:p.Ala198Thr
NM_032638.4:c.592G>A , LRG_295t2:c.592G>A	NP_116027.2:p.Ala198Thr
NM_001145661.2:c.592G>A MANE Plus Clinical	NP_001139133.1:p.Ala198Thr
NM_032638.5:c.592G>A MANE Select	NP_116027.2:p.Ala198Thr