Canonical Allele Identifier: CA1053362124

Gene: GATA2

Linked Data

• dbSNP Id: rs2068653116
• gnomAD v3: 3-128483234-A-G
• gnomAD v4: 3-128483234-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483234A>G , CM000665.2:g.128483234A>G	GRCh38
NC_000003.11:g.128202077A>G , CM000665.1:g.128202077A>G	GRCh37
NC_000003.10:g.129684767A>G	NCBI36
NG_029334.1:g.14954T>C , LRG_295:g.14954T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.1017+626T>C MANE Plus Clinical	ENSP00000417074.1:n.1017+626T>C
ENST00000696466.1:c.1299+626T>C	ENSP00000512647.1:n.1299+626T>C
ENST00000341105.7:c.1017+626T>C MANE Select	ENSP00000345681.2:n.1017+626T>C
ENST00000341105.6:c.1017+626T>C	ENSP00000345681.2:n.1017+626T>C
ENST00000430265.6:c.1017+626T>C	ENSP00000400259.2:n.1017+626T>C
ENST00000487848.5:c.1017+626T>C	ENSP00000417074.1:n.1017+626T>C
NM_001145661.1:c.1017+626T>C , LRG_295t1:c.1017+626T>C	NP_001139133.1:n.1017+626T>C
NM_001145662.1:c.1017+626T>C	NP_001139134.1:n.1017+626T>C
NM_032638.4:c.1017+626T>C , LRG_295t2:c.1017+626T>C	NP_116027.2:n.1017+626T>C
NM_001145661.2:c.1017+626T>C MANE Plus Clinical	NP_001139133.1:n.1017+626T>C
NM_032638.5:c.1017+626T>C MANE Select	NP_116027.2:n.1017+626T>C