Canonical Allele Identifier: CA1400719391
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128486100A= , CM000665.2:g.128486100A= GRCh38
NC_000003.11:g.128204943A= , CM000665.1:g.128204943A= GRCh37
NC_000003.10:g.129687633A= NCBI36
NG_029334.1:g.12088T= , LRG_295:g.12088T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.498T= MANE Plus Clinical ENSP00000417074.1:p.Ser166=
ENST00000696466.1:c.780T= ENSP00000512647.1:p.Ser260=
ENST00000341105.7:c.498T= MANE Select ENSP00000345681.2:p.Ser166=
ENST00000341105.6:c.498T= ENSP00000345681.2:p.Ser166=
ENST00000430265.6:c.498T= ENSP00000400259.2:p.Ser166=
ENST00000487848.5:c.498T= ENSP00000417074.1:p.Ser166=
NM_001145661.1:c.498T= , LRG_295t1:c.498T= NP_001139133.1:p.Ser166=
NM_001145662.1:c.498T= NP_001139134.1:p.Ser166=
NM_032638.4:c.498T= , LRG_295t2:c.498T= NP_116027.2:p.Ser166=
NM_001145661.2:c.498T= MANE Plus Clinical NP_001139133.1:p.Ser166=
NM_032638.5:c.498T= MANE Select NP_116027.2:p.Ser166=