Canonical Allele Identifier: CA354412419

Gene: GATA2

Linked Data

• ClinVar Variation Id: 2941922
• ClinVar RCV Id: RCV003802944
• dbSNP Id: rs1161135105
• gnomAD v2: 3-128199879-C-T
• MyVariant Identifiers: chr3:g.128199879C>T (hg19) ; chr3:g.128481036C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481036C>T , CM000665.2:g.128481036C>T	GRCh38
NC_000003.11:g.128199879C>T , CM000665.1:g.128199879C>T	GRCh37
NC_000003.10:g.129682569C>T	NCBI36
NG_029334.1:g.17152G>A , LRG_295:g.17152G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1426G>A MANE Plus Clinical	ENSP00000417074.1:p.Val476Met
ENST00000696466.1:c.1708G>A	ENSP00000512647.1:p.Val570Met
ENST00000696672.1:c.401G>A	ENSP00000512796.1:p.Gly134Asp
ENST00000341105.7:c.1426G>A MANE Select	ENSP00000345681.2:p.Val476Met
ENST00000341105.6:c.1426G>A	ENSP00000345681.2:p.Val476Met
ENST00000430265.6:c.1384G>A	ENSP00000400259.2:p.Val462Met
ENST00000487848.5:c.1426G>A	ENSP00000417074.1:p.Val476Met
ENST00000489987.1:n.543G>A
NM_001145661.1:c.1426G>A , LRG_295t1:c.1426G>A	NP_001139133.1:p.Val476Met
NM_001145662.1:c.1384G>A	NP_001139134.1:p.Val462Met
NM_032638.4:c.1426G>A , LRG_295t2:c.1426G>A	NP_116027.2:p.Val476Met
NM_001145661.2:c.1426G>A MANE Plus Clinical	NP_001139133.1:p.Val476Met
NM_032638.5:c.1426G>A MANE Select	NP_116027.2:p.Val476Met