Canonical Allele Identifier: CA898657385

Gene: GATA2 GATA2-AS1

Linked Data

• dbSNP Id: rs1402804018
• MyVariant Identifiers: chr3:g.128211359T>G (hg19) ; chr3:g.128492516T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128492516T>G , CM000665.2:g.128492516T>G	GRCh38
NC_000003.11:g.128211359T>G , CM000665.1:g.128211359T>G	GRCh37
NC_000003.10:g.129694049T>G	NCBI36
NG_029334.1:g.5672A>C , LRG_295:g.5672A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696466.1:c.-193-294A>C (GATA2)	ENSP00000512647.1:n.-193-294A>C
ENST00000696654.1:c.-598-294A>C (GATA2)	ENSP00000512783.1:n.-598-294A>C
ENST00000696655.1:n.288+383A>C (GATA2)
ENST00000341105.7:c.-46+383A>C (GATA2) MANE Select	ENSP00000345681.2:n.-46+383A>C
ENST00000341105.6:c.-46+383A>C (GATA2)	ENSP00000345681.2:n.-46+383A>C
ENST00000498200.1:c.-264-294A>C (GATA2)	ENSP00000419532.1:n.-264-294A>C
NM_032638.4:c.-46+383A>C , LRG_295t2:c.-46+383A>C (GATA2)	NP_116027.2:n.-46+383A>C
NR_125398.1:n.759+2447T>G (GATA2-AS1)
NM_032638.5:c.-46+383A>C (GATA2) MANE Select	NP_116027.2:n.-46+383A>C