Canonical Allele Identifier: CA2667539874

Gene: GATA2

Linked Data

• gnomAD v4: 3-128480641-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480641A>C , CM000665.2:g.128480641A>C	GRCh38
NC_000003.11:g.128199484A>C , CM000665.1:g.128199484A>C	GRCh37
NC_000003.10:g.129682174A>C	NCBI36
NG_029334.1:g.17547T>G , LRG_295:g.17547T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.*378T>G MANE Plus Clinical	ENSP00000417074.1:n.*378T>G
ENST00000696466.1:c.*378T>G	ENSP00000512647.1:n.*378T>G
ENST00000696672.1:c.796T>G	ENSP00000512796.1:n.796T>G
ENST00000341105.7:c.*378T>G MANE Select	ENSP00000345681.2:n.*378T>G
ENST00000341105.6:c.*378T>G	ENSP00000345681.2:n.*378T>G
ENST00000430265.6:c.*378T>G	ENSP00000400259.2:n.*378T>G
ENST00000489987.1:n.938T>G
NM_001145661.1:c.*378T>G , LRG_295t1:c.*378T>G	NP_001139133.1:n.*378T>G
NM_001145662.1:c.*378T>G	NP_001139134.1:n.*378T>G
NM_032638.4:c.*378T>G , LRG_295t2:c.*378T>G	NP_116027.2:n.*378T>G
NM_001145661.2:c.*378T>G MANE Plus Clinical	NP_001139133.1:n.*378T>G
NM_032638.5:c.*378T>G MANE Select	NP_116027.2:n.*378T>G