Canonical Allele Identifier: CA1400716832

Gene: GATA2

Linked Data

• ClinVar Variation Id: 1094331
• ClinVar RCV Id: RCV001414790
• dbSNP Id: rs890419135

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128483348G>C , CM000665.2:g.128483348G>C	GRCh38
NC_000003.11:g.128202191G>C , CM000665.1:g.128202191G>C	GRCh37
NC_000003.10:g.129684881G>C	NCBI36
NG_029334.1:g.14840C>G , LRG_295:g.14840C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1017+512C>G MANE Plus Clinical	ENSP00000417074.1:n.1017+512C>G
ENST00000696466.1:c.1299+512C>G	ENSP00000512647.1:n.1299+512C>G
ENST00000341105.7:c.1017+512C>G MANE Select	ENSP00000345681.2:n.1017+512C>G
ENST00000341105.6:c.1017+512C>G	ENSP00000345681.2:n.1017+512C>G
ENST00000430265.6:c.1017+512C>G	ENSP00000400259.2:n.1017+512C>G
ENST00000487848.5:c.1017+512C>G	ENSP00000417074.1:n.1017+512C>G
NM_001145661.1:c.1017+512C>G , LRG_295t1:c.1017+512C>G	NP_001139133.1:n.1017+512C>G
NM_001145662.1:c.1017+512C>G	NP_001139134.1:n.1017+512C>G
NM_032638.4:c.1017+512C>G , LRG_295t2:c.1017+512C>G	NP_116027.2:n.1017+512C>G
NM_001145661.2:c.1017+512C>G MANE Plus Clinical	NP_001139133.1:n.1017+512C>G
NM_032638.5:c.1017+512C>G MANE Select	NP_116027.2:n.1017+512C>G