Canonical Allele Identifier: CA354412499

Gene: GATA2

Linked Data

• dbSNP Id: rs2107667668
• MyVariant Identifiers: chr3:g.128199902C>A (hg19) ; chr3:g.128481059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481059C>A , CM000665.2:g.128481059C>A	GRCh38
NC_000003.11:g.128199902C>A , CM000665.1:g.128199902C>A	GRCh37
NC_000003.10:g.129682592C>A	NCBI36
NG_029334.1:g.17129G>T , LRG_295:g.17129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1403G>T MANE Plus Clinical	ENSP00000417074.1:p.Gly468Val
ENST00000696466.1:c.1685G>T	ENSP00000512647.1:p.Gly562Val
ENST00000696672.1:c.378G>T	ENSP00000512796.1:p.Arg126=
ENST00000341105.7:c.1403G>T MANE Select	ENSP00000345681.2:p.Gly468Val
ENST00000341105.6:c.1403G>T	ENSP00000345681.2:p.Gly468Val
ENST00000430265.6:c.1361G>T	ENSP00000400259.2:p.Gly454Val
ENST00000487848.5:c.1403G>T	ENSP00000417074.1:p.Gly468Val
ENST00000489987.1:n.520G>T
NM_001145661.1:c.1403G>T , LRG_295t1:c.1403G>T	NP_001139133.1:p.Gly468Val
NM_001145662.1:c.1361G>T	NP_001139134.1:p.Gly454Val
NM_032638.4:c.1403G>T , LRG_295t2:c.1403G>T	NP_116027.2:p.Gly468Val
NM_001145661.2:c.1403G>T MANE Plus Clinical	NP_001139133.1:p.Gly468Val
NM_032638.5:c.1403G>T MANE Select	NP_116027.2:p.Gly468Val