Canonical Allele Identifier: CA2599763
Gene: GATA2 HGNC NCBI

Linked Data

dbSNP Id: rs371094127

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480985C>T , CM000665.2:g.128480985C>T GRCh38
NC_000003.11:g.128199828C>T , CM000665.1:g.128199828C>T GRCh37
NC_000003.10:g.129682518C>T NCBI36
NG_029334.1:g.17203G>A , LRG_295:g.17203G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.*34G>A MANE Plus Clinical ENSP00000417074.1:n.*34G>A
ENST00000696466.1:c.*34G>A ENSP00000512647.1:n.*34G>A
ENST00000696672.1:c.452G>A ENSP00000512796.1:p.Arg151Gln
ENST00000341105.7:c.*34G>A MANE Select ENSP00000345681.2:n.*34G>A
ENST00000341105.6:c.*34G>A ENSP00000345681.2:n.*34G>A
ENST00000430265.6:c.*34G>A ENSP00000400259.2:n.*34G>A
ENST00000489987.1:n.594G>A
NM_001145661.1:c.*34G>A , LRG_295t1:c.*34G>A NP_001139133.1:n.*34G>A
NM_001145662.1:c.*34G>A NP_001139134.1:n.*34G>A
NM_032638.4:c.*34G>A , LRG_295t2:c.*34G>A NP_116027.2:n.*34G>A
NM_001145661.2:c.*34G>A MANE Plus Clinical NP_001139133.1:n.*34G>A
NM_032638.5:c.*34G>A MANE Select NP_116027.2:n.*34G>A