Canonical Allele Identifier: CA128584

Gene: GATA2

Linked Data

• ClinVar Variation Id: 29719
• ClinVar RCV Id: RCV000022571 ; RCV000812052 ; RCV000984812 ; RCV001542112
• dbSNP Id: rs387906632
• COSMIC: COSM6022403
• MyVariant Identifiers: chr3:g.128202711G>A (hg19) ; chr3:g.128483868G>A (hg38)
• PubMed: PMID:21892158

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483868G>A , CM000665.2:g.128483868G>A	GRCh38
NC_000003.11:g.128202711G>A , CM000665.1:g.128202711G>A	GRCh37
NC_000003.10:g.129685401G>A	NCBI36
NG_029334.1:g.14320C>T , LRG_295:g.14320C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.1009C>T MANE Plus Clinical	ENSP00000417074.1:p.Arg337Ter
ENST00000696466.1:c.1291C>T	ENSP00000512647.1:p.Arg431Ter
ENST00000341105.7:c.1009C>T MANE Select	ENSP00000345681.2:p.Arg337Ter
ENST00000341105.6:c.1009C>T	ENSP00000345681.2:p.Arg337Ter
ENST00000430265.6:c.1009C>T	ENSP00000400259.2:p.Arg337Ter
ENST00000487848.5:c.1009C>T	ENSP00000417074.1:p.Arg337Ter
NM_001145661.1:c.1009C>T , LRG_295t1:c.1009C>T	NP_001139133.1:p.Arg337Ter
NM_001145662.1:c.1009C>T	NP_001139134.1:p.Arg337Ter
NM_032638.4:c.1009C>T , LRG_295t2:c.1009C>T	NP_116027.2:p.Arg337Ter
NM_001145661.2:c.1009C>T MANE Plus Clinical	NP_001139133.1:p.Arg337Ter
NM_032638.5:c.1009C>T MANE Select	NP_116027.2:p.Arg337Ter