Canonical Allele Identifier: CA435763786

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1092008
• ClinVar RCV Id: RCV001411675
• dbSNP Id: rs1363204381
• MyVariant Identifiers: chr3:g.128204949G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128486106G>C , CM000665.2:g.128486106G>C	GRCh38
NC_000003.11:g.128204949G>C , CM000665.1:g.128204949G>C	GRCh37
NC_000003.10:g.129687639G>C	NCBI36
NG_029334.1:g.12082C>G , LRG_295:g.12082C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.492C>G MANE Plus Clinical	ENSP00000417074.1:p.Ala164=
ENST00000696466.1:c.774C>G	ENSP00000512647.1:p.Ala258=
ENST00000341105.7:c.492C>G MANE Select	ENSP00000345681.2:p.Ala164=
ENST00000341105.6:c.492C>G	ENSP00000345681.2:p.Ala164=
ENST00000430265.6:c.492C>G	ENSP00000400259.2:p.Ala164=
ENST00000487848.5:c.492C>G	ENSP00000417074.1:p.Ala164=
NM_001145661.1:c.492C>G , LRG_295t1:c.492C>G	NP_001139133.1:p.Ala164=
NM_001145662.1:c.492C>G	NP_001139134.1:p.Ala164=
NM_032638.4:c.492C>G , LRG_295t2:c.492C>G	NP_116027.2:p.Ala164=
NM_001145661.2:c.492C>G MANE Plus Clinical	NP_001139133.1:p.Ala164=
NM_032638.5:c.492C>G MANE Select	NP_116027.2:p.Ala164=