Canonical Allele Identifier: CA2667539852
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480627T>C , CM000665.2:g.128480627T>C GRCh38
NC_000003.11:g.128199470T>C , CM000665.1:g.128199470T>C GRCh37
NC_000003.10:g.129682160T>C NCBI36
NG_029334.1:g.17561A>G , LRG_295:g.17561A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.*392A>G MANE Plus Clinical ENSP00000417074.1:n.*392A>G
ENST00000696466.1:c.*392A>G ENSP00000512647.1:n.*392A>G
ENST00000696672.1:c.810A>G ENSP00000512796.1:n.810A>G
ENST00000341105.7:c.*392A>G MANE Select ENSP00000345681.2:n.*392A>G
ENST00000341105.6:c.*392A>G ENSP00000345681.2:n.*392A>G
ENST00000430265.6:c.*392A>G ENSP00000400259.2:n.*392A>G
ENST00000489987.1:n.952A>G
NM_001145661.1:c.*392A>G , LRG_295t1:c.*392A>G NP_001139133.1:n.*392A>G
NM_001145662.1:c.*392A>G NP_001139134.1:n.*392A>G
NM_032638.4:c.*392A>G , LRG_295t2:c.*392A>G NP_116027.2:n.*392A>G
NM_001145661.2:c.*392A>G MANE Plus Clinical NP_001139133.1:n.*392A>G
NM_032638.5:c.*392A>G MANE Select NP_116027.2:n.*392A>G