Canonical Allele Identifier: CA435510012

Gene: GATA2

Linked Data

• MyVariant Identifiers: chr3:g.128202798G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483955G>T , CM000665.2:g.128483955G>T	GRCh38
NC_000003.11:g.128202798G>T , CM000665.1:g.128202798G>T	GRCh37
NC_000003.10:g.129685488G>T	NCBI36
NG_029334.1:g.14233C>A , LRG_295:g.14233C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.922C>A MANE Plus Clinical	ENSP00000417074.1:p.Arg308=
ENST00000696466.1:c.1204C>A	ENSP00000512647.1:p.Arg402=
ENST00000341105.7:c.922C>A MANE Select	ENSP00000345681.2:p.Arg308=
ENST00000341105.6:c.922C>A	ENSP00000345681.2:p.Arg308=
ENST00000430265.6:c.922C>A	ENSP00000400259.2:p.Arg308=
ENST00000487848.5:c.922C>A	ENSP00000417074.1:p.Arg308=
NM_001145661.1:c.922C>A , LRG_295t1:c.922C>A	NP_001139133.1:p.Arg308=
NM_001145662.1:c.922C>A	NP_001139134.1:p.Arg308=
NM_032638.4:c.922C>A , LRG_295t2:c.922C>A	NP_116027.2:p.Arg308=
NM_001145661.2:c.922C>A MANE Plus Clinical	NP_001139133.1:p.Arg308=
NM_032638.5:c.922C>A MANE Select	NP_116027.2:p.Arg308=