Canonical Allele Identifier: CA1139533057
Gene: GATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1184021
ClinVar RCV Id: RCV001541971 RCV002568255
dbSNP Id: rs2107669881
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128483328A>T , CM000665.2:g.128483328A>T GRCh38
NC_000003.11:g.128202171A>T , CM000665.1:g.128202171A>T GRCh37
NC_000003.10:g.129684861A>T NCBI36
NG_029334.1:g.14860T>A , LRG_295:g.14860T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.1017+532T>A MANE Plus Clinical ENSP00000417074.1:n.1017+532T>A
ENST00000696466.1:c.1299+532T>A ENSP00000512647.1:n.1299+532T>A
ENST00000341105.7:c.1017+532T>A MANE Select ENSP00000345681.2:n.1017+532T>A
ENST00000341105.6:c.1017+532T>A ENSP00000345681.2:n.1017+532T>A
ENST00000430265.6:c.1017+532T>A ENSP00000400259.2:n.1017+532T>A
ENST00000487848.5:c.1017+532T>A ENSP00000417074.1:n.1017+532T>A
NM_001145661.1:c.1017+532T>A , LRG_295t1:c.1017+532T>A NP_001139133.1:n.1017+532T>A
NM_001145662.1:c.1017+532T>A NP_001139134.1:n.1017+532T>A
NM_032638.4:c.1017+532T>A , LRG_295t2:c.1017+532T>A NP_116027.2:n.1017+532T>A
NM_001145661.2:c.1017+532T>A MANE Plus Clinical NP_001139133.1:n.1017+532T>A
NM_032638.5:c.1017+532T>A MANE Select NP_116027.2:n.1017+532T>A
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