Canonical Allele Identifier: CA435509986

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1095421
• ClinVar RCV Id: RCV001416317
• dbSNP Id: rs2107670374
• MyVariant Identifiers: chr3:g.128202757G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483914G>C , CM000665.2:g.128483914G>C	GRCh38
NC_000003.11:g.128202757G>C , CM000665.1:g.128202757G>C	GRCh37
NC_000003.10:g.129685447G>C	NCBI36
NG_029334.1:g.14274C>G , LRG_295:g.14274C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.963C>G MANE Plus Clinical	ENSP00000417074.1:p.Leu321=
ENST00000696466.1:c.1245C>G	ENSP00000512647.1:p.Leu415=
ENST00000341105.7:c.963C>G MANE Select	ENSP00000345681.2:p.Leu321=
ENST00000341105.6:c.963C>G	ENSP00000345681.2:p.Leu321=
ENST00000430265.6:c.963C>G	ENSP00000400259.2:p.Leu321=
ENST00000487848.5:c.963C>G	ENSP00000417074.1:p.Leu321=
NM_001145661.1:c.963C>G , LRG_295t1:c.963C>G	NP_001139133.1:p.Leu321=
NM_001145662.1:c.963C>G	NP_001139134.1:p.Leu321=
NM_032638.4:c.963C>G , LRG_295t2:c.963C>G	NP_116027.2:p.Leu321=
NM_001145661.2:c.963C>G MANE Plus Clinical	NP_001139133.1:p.Leu321=
NM_032638.5:c.963C>G MANE Select	NP_116027.2:p.Leu321=