Canonical Allele Identifier: CA1400714768

Gene: GATA2

Linked Data

• dbSNP Id: rs2068629474

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481620A>T , CM000665.2:g.128481620A>T	GRCh38
NC_000003.11:g.128200463A>T , CM000665.1:g.128200463A>T	GRCh37
NC_000003.10:g.129683153A>T	NCBI36
NG_029334.1:g.16568T>A , LRG_295:g.16568T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.1143+199T>A MANE Plus Clinical	ENSP00000417074.1:n.1143+199T>A
ENST00000696466.1:c.1425+199T>A	ENSP00000512647.1:n.1425+199T>A
ENST00000696672.1:c.126+199T>A	ENSP00000512796.1:n.126+199T>A
ENST00000341105.7:c.1143+199T>A MANE Select	ENSP00000345681.2:n.1143+199T>A
ENST00000341105.6:c.1143+199T>A	ENSP00000345681.2:n.1143+199T>A
ENST00000430265.6:c.1101+199T>A	ENSP00000400259.2:n.1101+199T>A
ENST00000487848.5:c.1143+199T>A	ENSP00000417074.1:n.1143+199T>A
ENST00000489987.1:n.260+199T>A
NM_001145661.1:c.1143+199T>A , LRG_295t1:c.1143+199T>A	NP_001139133.1:n.1143+199T>A
NM_001145662.1:c.1101+199T>A	NP_001139134.1:n.1101+199T>A
NM_032638.4:c.1143+199T>A , LRG_295t2:c.1143+199T>A	NP_116027.2:n.1143+199T>A
NM_001145661.2:c.1143+199T>A MANE Plus Clinical	NP_001139133.1:n.1143+199T>A
NM_032638.5:c.1143+199T>A MANE Select	NP_116027.2:n.1143+199T>A