Canonical Allele Identifier: CA1400717299
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128483811C= , CM000665.2:g.128483811C= GRCh38
NC_000003.11:g.128202654C= , CM000665.1:g.128202654C= GRCh37
NC_000003.10:g.129685344C= NCBI36
NG_029334.1:g.14377G= , LRG_295:g.14377G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.1017+49G= MANE Plus Clinical ENSP00000417074.1:n.1017+49G=
ENST00000696466.1:c.1299+49G= ENSP00000512647.1:n.1299+49G=
ENST00000341105.7:c.1017+49G= MANE Select ENSP00000345681.2:n.1017+49G=
ENST00000341105.6:c.1017+49G= ENSP00000345681.2:n.1017+49G=
ENST00000430265.6:c.1017+49G= ENSP00000400259.2:n.1017+49G=
ENST00000487848.5:c.1017+49G= ENSP00000417074.1:n.1017+49G=
NM_001145661.1:c.1017+49G= , LRG_295t1:c.1017+49G= NP_001139133.1:n.1017+49G=
NM_001145662.1:c.1017+49G= NP_001139134.1:n.1017+49G=
NM_032638.4:c.1017+49G= , LRG_295t2:c.1017+49G= NP_116027.2:n.1017+49G=
NM_001145661.2:c.1017+49G= MANE Plus Clinical NP_001139133.1:n.1017+49G=
NM_032638.5:c.1017+49G= MANE Select NP_116027.2:n.1017+49G=