Canonical Allele Identifier: CA354404802
Gene: GATA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956340
dbSNP Id: rs1237462942

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128483972G>A , CM000665.2:g.128483972G>A GRCh38
NC_000003.11:g.128202815G>A , CM000665.1:g.128202815G>A GRCh37
NC_000003.10:g.129685505G>A NCBI36
NG_029334.1:g.14216C>T , LRG_295:g.14216C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.905C>T MANE Plus Clinical ENSP00000417074.1:p.Ala302Val
ENST00000696466.1:c.1187C>T ENSP00000512647.1:p.Ala396Val
ENST00000341105.7:c.905C>T MANE Select ENSP00000345681.2:p.Ala302Val
ENST00000341105.6:c.905C>T ENSP00000345681.2:p.Ala302Val
ENST00000430265.6:c.905C>T ENSP00000400259.2:p.Ala302Val
ENST00000487848.5:c.905C>T ENSP00000417074.1:p.Ala302Val
NM_001145661.1:c.905C>T , LRG_295t1:c.905C>T NP_001139133.1:p.Ala302Val
NM_001145662.1:c.905C>T NP_001139134.1:p.Ala302Val
NM_032638.4:c.905C>T , LRG_295t2:c.905C>T NP_116027.2:p.Ala302Val
NM_001145661.2:c.905C>T MANE Plus Clinical NP_001139133.1:p.Ala302Val
NM_032638.5:c.905C>T MANE Select NP_116027.2:p.Ala302Val