Canonical Allele Identifier: CA354406822

Gene: GATA2

Linked Data

• ClinVar Variation Id: 644139
• ClinVar RCV Id: RCV000797991
• dbSNP Id: rs1576749003
• MyVariant Identifiers: chr3:g.128205022A>G (hg19) ; chr3:g.128486179A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128486179A>G , CM000665.2:g.128486179A>G	GRCh38
NC_000003.11:g.128205022A>G , CM000665.1:g.128205022A>G	GRCh37
NC_000003.10:g.129687712A>G	NCBI36
NG_029334.1:g.12009T>C , LRG_295:g.12009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.419T>C MANE Plus Clinical	ENSP00000417074.1:p.Val140Ala
ENST00000696466.1:c.701T>C	ENSP00000512647.1:p.Val234Ala
ENST00000341105.7:c.419T>C MANE Select	ENSP00000345681.2:p.Val140Ala
ENST00000341105.6:c.419T>C	ENSP00000345681.2:p.Val140Ala
ENST00000430265.6:c.419T>C	ENSP00000400259.2:p.Val140Ala
ENST00000487848.5:c.419T>C	ENSP00000417074.1:p.Val140Ala
ENST00000492608.1:c.419T>C	ENSP00000418132.1:p.Val140Ala
NM_001145661.1:c.419T>C , LRG_295t1:c.419T>C	NP_001139133.1:p.Val140Ala
NM_001145662.1:c.419T>C	NP_001139134.1:p.Val140Ala
NM_032638.4:c.419T>C , LRG_295t2:c.419T>C	NP_116027.2:p.Val140Ala
NM_001145661.2:c.419T>C MANE Plus Clinical	NP_001139133.1:p.Val140Ala
NM_032638.5:c.419T>C MANE Select	NP_116027.2:p.Val140Ala