Canonical Allele Identifier: CA1400719470
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128486233G= , CM000665.2:g.128486233G= GRCh38
NC_000003.11:g.128205076G= , CM000665.1:g.128205076G= GRCh37
NC_000003.10:g.129687766G= NCBI36
NG_029334.1:g.11955C= , LRG_295:g.11955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.365C= MANE Plus Clinical ENSP00000417074.1:p.Ser122=
ENST00000696466.1:c.647C= ENSP00000512647.1:p.Ser216=
ENST00000341105.7:c.365C= MANE Select ENSP00000345681.2:p.Ser122=
ENST00000341105.6:c.365C= ENSP00000345681.2:p.Ser122=
ENST00000430265.6:c.365C= ENSP00000400259.2:p.Ser122=
ENST00000487848.5:c.365C= ENSP00000417074.1:p.Ser122=
ENST00000492608.1:c.365C= ENSP00000418132.1:p.Ser122=
NM_001145661.1:c.365C= , LRG_295t1:c.365C= NP_001139133.1:p.Ser122=
NM_001145662.1:c.365C= NP_001139134.1:p.Ser122=
NM_032638.4:c.365C= , LRG_295t2:c.365C= NP_116027.2:p.Ser122=
NM_001145661.2:c.365C= MANE Plus Clinical NP_001139133.1:p.Ser122=
NM_032638.5:c.365C= MANE Select NP_116027.2:p.Ser122=