Canonical Allele Identifier: CA354413617

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1184242
• ClinVar RCV Id: RCV001542227
• dbSNP Id: rs387906631
• gnomAD v4: 3-128481901-G-C
• COSMIC: COSM5985185
• MyVariant Identifiers: chr3:g.128200744G>C (hg19) ; chr3:g.128481901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481901G>C , CM000665.2:g.128481901G>C	GRCh38
NC_000003.11:g.128200744G>C , CM000665.1:g.128200744G>C	GRCh37
NC_000003.10:g.129683434G>C	NCBI36
NG_029334.1:g.16287C>G , LRG_295:g.16287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1061C>G MANE Plus Clinical	ENSP00000417074.1:p.Thr354Arg
ENST00000696466.1:c.1343C>G	ENSP00000512647.1:p.Thr448Arg
ENST00000696672.1:c.44C>G	ENSP00000512796.1:p.Thr15Arg
ENST00000341105.7:c.1061C>G MANE Select	ENSP00000345681.2:p.Thr354Arg
ENST00000341105.6:c.1061C>G	ENSP00000345681.2:p.Thr354Arg
ENST00000430265.6:c.1019C>G	ENSP00000400259.2:p.Thr340Arg
ENST00000487848.5:c.1061C>G	ENSP00000417074.1:p.Thr354Arg
ENST00000489987.1:n.178C>G
NM_001145661.1:c.1061C>G , LRG_295t1:c.1061C>G	NP_001139133.1:p.Thr354Arg
NM_001145662.1:c.1019C>G	NP_001139134.1:p.Thr340Arg
NM_032638.4:c.1061C>G , LRG_295t2:c.1061C>G	NP_116027.2:p.Thr354Arg
NM_001145661.2:c.1061C>G MANE Plus Clinical	NP_001139133.1:p.Thr354Arg
NM_032638.5:c.1061C>G MANE Select	NP_116027.2:p.Thr354Arg