Canonical Allele Identifier: CA1400712654
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480043T= , CM000665.2:g.128480043T= GRCh38
NC_000003.11:g.128198886T= , CM000665.1:g.128198886T= GRCh37
NC_000003.10:g.129681576T= NCBI36
NG_029334.1:g.18145A= , LRG_295:g.18145A=

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.*976A= MANE Plus Clinical ENSP00000417074.1:n.*976A=
ENST00000696466.1:c.*976A= ENSP00000512647.1:n.*976A=
ENST00000696672.1:c.1394A= ENSP00000512796.1:n.1394A=
ENST00000341105.7:c.*976A= MANE Select ENSP00000345681.2:n.*976A=
ENST00000341105.6:c.*976A= ENSP00000345681.2:n.*976A=
NM_001145661.1:c.*976A= , LRG_295t1:c.*976A= NP_001139133.1:n.*976A=
NM_001145662.1:c.*976A= NP_001139134.1:n.*976A=
NM_032638.4:c.*976A= , LRG_295t2:c.*976A= NP_116027.2:n.*976A=
NM_001145661.2:c.*976A= MANE Plus Clinical NP_001139133.1:n.*976A=
NM_032638.5:c.*976A= MANE Select NP_116027.2:n.*976A=