Canonical Allele Identifier: CA354412874

Gene: GATA2

Linked Data

• ClinVar Variation Id: 848285
• ClinVar RCV Id: RCV001052008
• dbSNP Id: rs2068623217
• MyVariant Identifiers: chr3:g.128200025G>C (hg19) ; chr3:g.128481182G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481182G>C , CM000665.2:g.128481182G>C	GRCh38
NC_000003.11:g.128200025G>C , CM000665.1:g.128200025G>C	GRCh37
NC_000003.10:g.129682715G>C	NCBI36
NG_029334.1:g.17006C>G , LRG_295:g.17006C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1280C>G MANE Plus Clinical	ENSP00000417074.1:p.Pro427Arg
ENST00000696466.1:c.1562C>G	ENSP00000512647.1:p.Pro521Arg
ENST00000696672.1:c.255C>G	ENSP00000512796.1:p.Pro85=
ENST00000341105.7:c.1280C>G MANE Select	ENSP00000345681.2:p.Pro427Arg
ENST00000341105.6:c.1280C>G	ENSP00000345681.2:p.Pro427Arg
ENST00000430265.6:c.1238C>G	ENSP00000400259.2:p.Pro413Arg
ENST00000487848.5:c.1280C>G	ENSP00000417074.1:p.Pro427Arg
ENST00000489987.1:n.397C>G
NM_001145661.1:c.1280C>G , LRG_295t1:c.1280C>G	NP_001139133.1:p.Pro427Arg
NM_001145662.1:c.1238C>G	NP_001139134.1:p.Pro413Arg
NM_032638.4:c.1280C>G , LRG_295t2:c.1280C>G	NP_116027.2:p.Pro427Arg
NM_001145661.2:c.1280C>G MANE Plus Clinical	NP_001139133.1:p.Pro427Arg
NM_032638.5:c.1280C>G MANE Select	NP_116027.2:p.Pro427Arg