Canonical Allele Identifier: CA354413477

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1184193
• ClinVar RCV Id: RCV001821863
• dbSNP Id: rs2107668593
• MyVariant Identifiers: chr3:g.128200676A>C (hg19) ; chr3:g.128481833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481833A>C , CM000665.2:g.128481833A>C	GRCh38
NC_000003.11:g.128200676A>C , CM000665.1:g.128200676A>C	GRCh37
NC_000003.10:g.129683366A>C	NCBI36
NG_029334.1:g.16355T>G , LRG_295:g.16355T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.1129T>G MANE Plus Clinical	ENSP00000417074.1:p.Tyr377Asp
ENST00000696466.1:c.1411T>G	ENSP00000512647.1:p.Tyr471Asp
ENST00000696672.1:c.112T>G	ENSP00000512796.1:p.Tyr38Asp
ENST00000341105.7:c.1129T>G MANE Select	ENSP00000345681.2:p.Tyr377Asp
ENST00000341105.6:c.1129T>G	ENSP00000345681.2:p.Tyr377Asp
ENST00000430265.6:c.1087T>G	ENSP00000400259.2:p.Tyr363Asp
ENST00000487848.5:c.1129T>G	ENSP00000417074.1:p.Tyr377Asp
ENST00000489987.1:n.246T>G
NM_001145661.1:c.1129T>G , LRG_295t1:c.1129T>G	NP_001139133.1:p.Tyr377Asp
NM_001145662.1:c.1087T>G	NP_001139134.1:p.Tyr363Asp
NM_032638.4:c.1129T>G , LRG_295t2:c.1129T>G	NP_116027.2:p.Tyr377Asp
NM_001145661.2:c.1129T>G MANE Plus Clinical	NP_001139133.1:p.Tyr377Asp
NM_032638.5:c.1129T>G MANE Select	NP_116027.2:p.Tyr377Asp