Canonical Allele Identifier: CA83371979
Gene: GATA2 HGNC NCBI

Linked Data

dbSNP Id: rs17844950

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128486107G>C , CM000665.2:g.128486107G>C GRCh38
NC_000003.11:g.128204950G>C , CM000665.1:g.128204950G>C GRCh37
NC_000003.10:g.129687640G>C NCBI36
NG_029334.1:g.12081C>G , LRG_295:g.12081C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.491C>G MANE Plus Clinical ENSP00000417074.1:p.Ala164Gly
ENST00000696466.1:c.773C>G ENSP00000512647.1:p.Ala258Gly
ENST00000341105.7:c.491C>G MANE Select ENSP00000345681.2:p.Ala164Gly
ENST00000341105.6:c.491C>G ENSP00000345681.2:p.Ala164Gly
ENST00000430265.6:c.491C>G ENSP00000400259.2:p.Ala164Gly
ENST00000487848.5:c.491C>G ENSP00000417074.1:p.Ala164Gly
NM_001145661.1:c.491C>G , LRG_295t1:c.491C>G NP_001139133.1:p.Ala164Gly
NM_001145662.1:c.491C>G NP_001139134.1:p.Ala164Gly
NM_032638.4:c.491C>G , LRG_295t2:c.491C>G NP_116027.2:p.Ala164Gly
NM_001145661.2:c.491C>G MANE Plus Clinical NP_001139133.1:p.Ala164Gly
NM_032638.5:c.491C>G MANE Select NP_116027.2:p.Ala164Gly