Canonical Allele Identifier: CA2667540233

Gene: GATA2

Linked Data

• gnomAD v4: 3-128480976-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480976C>A , CM000665.2:g.128480976C>A	GRCh38
NC_000003.11:g.128199819C>A , CM000665.1:g.128199819C>A	GRCh37
NC_000003.10:g.129682509C>A	NCBI36
NG_029334.1:g.17212G>T , LRG_295:g.17212G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.*43G>T MANE Plus Clinical	ENSP00000417074.1:n.*43G>T
ENST00000696466.1:c.*43G>T	ENSP00000512647.1:n.*43G>T
ENST00000696672.1:c.461G>T	ENSP00000512796.1:p.Trp154Leu
ENST00000341105.7:c.*43G>T MANE Select	ENSP00000345681.2:n.*43G>T
ENST00000341105.6:c.*43G>T	ENSP00000345681.2:n.*43G>T
ENST00000430265.6:c.*43G>T	ENSP00000400259.2:n.*43G>T
ENST00000489987.1:n.603G>T
NM_001145661.1:c.*43G>T , LRG_295t1:c.*43G>T	NP_001139133.1:n.*43G>T
NM_001145662.1:c.*43G>T	NP_001139134.1:n.*43G>T
NM_032638.4:c.*43G>T , LRG_295t2:c.*43G>T	NP_116027.2:n.*43G>T
NM_001145661.2:c.*43G>T MANE Plus Clinical	NP_001139133.1:n.*43G>T
NM_032638.5:c.*43G>T MANE Select	NP_116027.2:n.*43G>T