Canonical Allele Identifier: CA354406457
Gene: GATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649115
ClinVar RCV Id: RCV000803972
dbSNP Id: rs1576748685

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