Canonical Allele Identifier: CA375966972

Gene: GATA3

Linked Data

• ClinVar Variation Id: 2782541
• ClinVar RCV Id: RCV003664032
• MyVariant Identifiers: chr10:g.8100348A>G (hg19) ; chr10:g.8058385A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058385A>G , CM000672.2:g.8058385A>G	GRCh38
NC_000010.10:g.8100348A>G , CM000672.1:g.8100348A>G	GRCh37
NC_000010.9:g.8140354A>G	NCBI36
NG_015859.1:g.8682A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.322A>G	ENSP00000341619.3:p.Thr108Ala
ENST00000379328.9:c.322A>G MANE Select	ENSP00000368632.3:p.Thr108Ala
ENST00000481743.2:c.322A>G	ENSP00000493486.1:p.Thr108Ala
ENST00000346208.3:c.322A>G	ENSP00000341619.3:p.Thr108Ala
ENST00000379328.7:c.322A>G	ENSP00000368632.3:p.Thr108Ala
NM_001002295.1:c.322A>G	NP_001002295.1:p.Thr108Ala
NM_002051.2:c.322A>G	NP_002042.1:p.Thr108Ala
XM_005252442.2:c.322A>G	XP_005252499.1:p.Thr108Ala
XM_005252443.3:c.322A>G	XP_005252500.1:p.Thr108Ala
XM_005252443.5:c.322A>G	XP_005252500.1:p.Thr108Ala
NM_001002295.2:c.322A>G MANE Select	NP_001002295.1:p.Thr108Ala
NM_002051.3:c.322A>G	NP_002042.1:p.Thr108Ala