Canonical Allele Identifier: CA354405989

Gene: GATA2

Linked Data

• dbSNP Id: rs2107671982
• MyVariant Identifiers: chr3:g.128204674G>A (hg19) ; chr3:g.128485831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128485831G>A , CM000665.2:g.128485831G>A	GRCh38
NC_000003.11:g.128204674G>A , CM000665.1:g.128204674G>A	GRCh37
NC_000003.10:g.129687364G>A	NCBI36
NG_029334.1:g.12357C>T , LRG_295:g.12357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.767C>T MANE Plus Clinical	ENSP00000417074.1:p.Ala256Val
ENST00000696466.1:c.1049C>T	ENSP00000512647.1:p.Ala350Val
ENST00000341105.7:c.767C>T MANE Select	ENSP00000345681.2:p.Ala256Val
ENST00000341105.6:c.767C>T	ENSP00000345681.2:p.Ala256Val
ENST00000430265.6:c.767C>T	ENSP00000400259.2:p.Ala256Val
ENST00000487848.5:c.767C>T	ENSP00000417074.1:p.Ala256Val
NM_001145661.1:c.767C>T , LRG_295t1:c.767C>T	NP_001139133.1:p.Ala256Val
NM_001145662.1:c.767C>T	NP_001139134.1:p.Ala256Val
NM_032638.4:c.767C>T , LRG_295t2:c.767C>T	NP_116027.2:p.Ala256Val
NM_001145661.2:c.767C>T MANE Plus Clinical	NP_001139133.1:p.Ala256Val
NM_032638.5:c.767C>T MANE Select	NP_116027.2:p.Ala256Val