Canonical Allele Identifier: CA354405966

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1467453
• ClinVar RCV Id: RCV001970404
• dbSNP Id: rs1353328065
• MyVariant Identifiers: chr3:g.128204667G>T (hg19) ; chr3:g.128485824G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128485824G>T , CM000665.2:g.128485824G>T	GRCh38
NC_000003.11:g.128204667G>T , CM000665.1:g.128204667G>T	GRCh37
NC_000003.10:g.129687357G>T	NCBI36
NG_029334.1:g.12364C>A , LRG_295:g.12364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.774C>A MANE Plus Clinical	ENSP00000417074.1:p.His258Gln
ENST00000696466.1:c.1056C>A	ENSP00000512647.1:p.His352Gln
ENST00000341105.7:c.774C>A MANE Select	ENSP00000345681.2:p.His258Gln
ENST00000341105.6:c.774C>A	ENSP00000345681.2:p.His258Gln
ENST00000430265.6:c.774C>A	ENSP00000400259.2:p.His258Gln
ENST00000487848.5:c.774C>A	ENSP00000417074.1:p.His258Gln
NM_001145661.1:c.774C>A , LRG_295t1:c.774C>A	NP_001139133.1:p.His258Gln
NM_001145662.1:c.774C>A	NP_001139134.1:p.His258Gln
NM_032638.4:c.774C>A , LRG_295t2:c.774C>A	NP_116027.2:p.His258Gln
NM_001145661.2:c.774C>A MANE Plus Clinical	NP_001139133.1:p.His258Gln
NM_032638.5:c.774C>A MANE Select	NP_116027.2:p.His258Gln