Canonical Allele Identifier: CA2703921571

Gene: GATA2

Linked Data

• dbSNP Id: rs2107667313

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480682_128480684dup , CM000665.2:g.128480682_128480684dup	GRCh38
NC_000003.11:g.128199525_128199527dup , CM000665.1:g.128199525_128199527dup	GRCh37
NC_000003.10:g.129682215_129682217dup	NCBI36
NG_029334.1:g.17506_17508dup , LRG_295:g.17506_17508dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*337_*339dup MANE Plus Clinical	ENSP00000417074.1:n.*337_*339dup
ENST00000696466.1:c.*337_*339dup	ENSP00000512647.1:n.*337_*339dup
ENST00000696672.1:c.755_757dup	ENSP00000512796.1:n.755_757dup
ENST00000341105.7:c.*337_*339dup MANE Select	ENSP00000345681.2:n.*337_*339dup
ENST00000341105.6:c.*337_*339dup	ENSP00000345681.2:n.*337_*339dup
ENST00000430265.6:c.*337_*339dup	ENSP00000400259.2:n.*337_*339dup
ENST00000489987.1:n.897_899dup
NM_001145661.1:c.*337_*339dup , LRG_295t1:c.*337_*339dup	NP_001139133.1:n.*337_*339dup
NM_001145662.1:c.*337_*339dup	NP_001139134.1:n.*337_*339dup
NM_032638.4:c.*337_*339dup , LRG_295t2:c.*337_*339dup	NP_116027.2:n.*337_*339dup
NM_001145661.2:c.*337_*339dup MANE Plus Clinical	NP_001139133.1:n.*337_*339dup
NM_032638.5:c.*337_*339dup MANE Select	NP_116027.2:n.*337_*339dup