Canonical Allele Identifier: CA435524527

Gene: GATA2

Linked Data

• dbSNP Id: rs1479026838
• gnomAD v2: 3-128199997-G-A
• gnomAD v4: 3-128481154-G-A
• MyVariant Identifiers: chr3:g.128199997G>A (hg19) ; chr3:g.128481154G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481154G>A , CM000665.2:g.128481154G>A	GRCh38
NC_000003.11:g.128199997G>A , CM000665.1:g.128199997G>A	GRCh37
NC_000003.10:g.129682687G>A	NCBI36
NG_029334.1:g.17034C>T , LRG_295:g.17034C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1308C>T MANE Plus Clinical	ENSP00000417074.1:p.His436=
ENST00000696466.1:c.1590C>T	ENSP00000512647.1:p.His530=
ENST00000696672.1:c.283C>T	ENSP00000512796.1:p.His95Tyr
ENST00000341105.7:c.1308C>T MANE Select	ENSP00000345681.2:p.His436=
ENST00000341105.6:c.1308C>T	ENSP00000345681.2:p.His436=
ENST00000430265.6:c.1266C>T	ENSP00000400259.2:p.His422=
ENST00000487848.5:c.1308C>T	ENSP00000417074.1:p.His436=
ENST00000489987.1:n.425C>T
NM_001145661.1:c.1308C>T , LRG_295t1:c.1308C>T	NP_001139133.1:p.His436=
NM_001145662.1:c.1266C>T	NP_001139134.1:p.His422=
NM_032638.4:c.1308C>T , LRG_295t2:c.1308C>T	NP_116027.2:p.His436=
NM_001145661.2:c.1308C>T MANE Plus Clinical	NP_001139133.1:p.His436=
NM_032638.5:c.1308C>T MANE Select	NP_116027.2:p.His436=