Canonical Allele Identifier: CA898646104

Gene: GATA2

Linked Data

• dbSNP Id: rs545460836
• gnomAD v4: 3-128480820-G-A
• MyVariant Identifiers: chr3:g.128199663G>A (hg19) ; chr3:g.128480820G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480820G>A , CM000665.2:g.128480820G>A	GRCh38
NC_000003.11:g.128199663G>A , CM000665.1:g.128199663G>A	GRCh37
NC_000003.10:g.129682353G>A	NCBI36
NG_029334.1:g.17368C>T , LRG_295:g.17368C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*199C>T MANE Plus Clinical	ENSP00000417074.1:n.*199C>T
ENST00000696466.1:c.*199C>T	ENSP00000512647.1:n.*199C>T
ENST00000696672.1:c.617C>T	ENSP00000512796.1:n.617C>T
ENST00000341105.7:c.*199C>T MANE Select	ENSP00000345681.2:n.*199C>T
ENST00000341105.6:c.*199C>T	ENSP00000345681.2:n.*199C>T
ENST00000430265.6:c.*199C>T	ENSP00000400259.2:n.*199C>T
ENST00000489987.1:n.759C>T
NM_001145661.1:c.*199C>T , LRG_295t1:c.*199C>T	NP_001139133.1:n.*199C>T
NM_001145662.1:c.*199C>T	NP_001139134.1:n.*199C>T
NM_032638.4:c.*199C>T , LRG_295t2:c.*199C>T	NP_116027.2:n.*199C>T
NM_001145661.2:c.*199C>T MANE Plus Clinical	NP_001139133.1:n.*199C>T
NM_032638.5:c.*199C>T MANE Select	NP_116027.2:n.*199C>T