Canonical Allele Identifier: CA16611169
Gene: GATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404089
dbSNP Id: rs1060500092

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128481302G>T , CM000665.2:g.128481302G>T GRCh38
NC_000003.11:g.128200145G>T , CM000665.1:g.128200145G>T GRCh37
NC_000003.10:g.129682835G>T NCBI36
NG_029334.1:g.16886C>A , LRG_295:g.16886C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.1160C>A MANE Plus Clinical ENSP00000417074.1:p.Thr387Asn
ENST00000696466.1:c.1442C>A ENSP00000512647.1:p.Thr481Asn
ENST00000696672.1:c.135C>A ENSP00000512796.1:p.Asp45Glu
ENST00000341105.7:c.1160C>A MANE Select ENSP00000345681.2:p.Thr387Asn
ENST00000341105.6:c.1160C>A ENSP00000345681.2:p.Thr387Asn
ENST00000430265.6:c.1118C>A ENSP00000400259.2:p.Thr373Asn
ENST00000487848.5:c.1160C>A ENSP00000417074.1:p.Thr387Asn
ENST00000489987.1:n.277C>A
NM_001145661.1:c.1160C>A , LRG_295t1:c.1160C>A NP_001139133.1:p.Thr387Asn
NM_001145662.1:c.1118C>A NP_001139134.1:p.Thr373Asn
NM_032638.4:c.1160C>A , LRG_295t2:c.1160C>A NP_116027.2:p.Thr387Asn
NM_001145661.2:c.1160C>A MANE Plus Clinical NP_001139133.1:p.Thr387Asn
NM_032638.5:c.1160C>A MANE Select NP_116027.2:p.Thr387Asn