Canonical Allele Identifier: CA1053362081

Gene: GATA2

Linked Data

• dbSNP Id: rs1255750954
• gnomAD v3: 3-128483161-GA-G
• gnomAD v4: 3-128483161-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483167del , CM000665.2:g.128483167del	GRCh38
NC_000003.11:g.128202010del , CM000665.1:g.128202010del	GRCh37
NC_000003.10:g.129684700del	NCBI36
NG_029334.1:g.15026del , LRG_295:g.15026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1017+698del MANE Plus Clinical	ENSP00000417074.1:n.1017+698del
ENST00000696466.1:c.1299+698del	ENSP00000512647.1:n.1299+698del
ENST00000341105.7:c.1017+698del MANE Select	ENSP00000345681.2:n.1017+698del
ENST00000341105.6:c.1017+698del	ENSP00000345681.2:n.1017+698del
ENST00000430265.6:c.1017+698del	ENSP00000400259.2:n.1017+698del
ENST00000487848.5:c.1017+698del	ENSP00000417074.1:n.1017+698del
NM_001145661.1:c.1017+698del , LRG_295t1:c.1017+698del	NP_001139133.1:n.1017+698del
NM_001145662.1:c.1017+698del	NP_001139134.1:n.1017+698del
NM_032638.4:c.1017+698del , LRG_295t2:c.1017+698del	NP_116027.2:n.1017+698del
NM_001145661.2:c.1017+698del MANE Plus Clinical	NP_001139133.1:n.1017+698del
NM_032638.5:c.1017+698del MANE Select	NP_116027.2:n.1017+698del