Canonical Allele Identifier: CA1400718470

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128485225G= , CM000665.2:g.128485225G=	GRCh38
NC_000003.11:g.128204068G= , CM000665.1:g.128204068G=	GRCh37
NC_000003.10:g.129686758G=	NCBI36
NG_029334.1:g.12963C= , LRG_295:g.12963C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.871+502C= MANE Plus Clinical	ENSP00000417074.1:n.871+502C=
ENST00000696466.1:c.1153+502C=	ENSP00000512647.1:n.1153+502C=
ENST00000341105.7:c.871+502C= MANE Select	ENSP00000345681.2:n.871+502C=
ENST00000341105.6:c.871+502C=	ENSP00000345681.2:n.871+502C=
ENST00000430265.6:c.871+502C=	ENSP00000400259.2:n.871+502C=
ENST00000487848.5:c.871+502C=	ENSP00000417074.1:n.871+502C=
NM_001145661.1:c.871+502C= , LRG_295t1:c.871+502C=	NP_001139133.1:n.871+502C=
NM_001145662.1:c.871+502C=	NP_001139134.1:n.871+502C=
NM_032638.4:c.871+502C= , LRG_295t2:c.871+502C=	NP_116027.2:n.871+502C=
NM_001145661.2:c.871+502C= MANE Plus Clinical	NP_001139133.1:n.871+502C=
NM_032638.5:c.871+502C= MANE Select	NP_116027.2:n.871+502C=