Canonical Allele Identifier: CA375966922

Gene: GATA3

Linked Data

• gnomAD v4: 10-8058361-G-T
• MyVariant Identifiers: chr10:g.8100324G>T (hg19) ; chr10:g.8058361G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058361G>T , CM000672.2:g.8058361G>T	GRCh38
NC_000010.10:g.8100324G>T , CM000672.1:g.8100324G>T	GRCh37
NC_000010.9:g.8140330G>T	NCBI36
NG_015859.1:g.8658G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.298G>T	ENSP00000341619.3:p.Gly100Cys
ENST00000379328.9:c.298G>T MANE Select	ENSP00000368632.3:p.Gly100Cys
ENST00000481743.2:c.298G>T	ENSP00000493486.1:p.Gly100Cys
ENST00000346208.3:c.298G>T	ENSP00000341619.3:p.Gly100Cys
ENST00000379328.7:c.298G>T	ENSP00000368632.3:p.Gly100Cys
NM_001002295.1:c.298G>T	NP_001002295.1:p.Gly100Cys
NM_002051.2:c.298G>T	NP_002042.1:p.Gly100Cys
XM_005252442.2:c.298G>T	XP_005252499.1:p.Gly100Cys
XM_005252443.3:c.298G>T	XP_005252500.1:p.Gly100Cys
XM_005252443.5:c.298G>T	XP_005252500.1:p.Gly100Cys
NM_001002295.2:c.298G>T MANE Select	NP_001002295.1:p.Gly100Cys
NM_002051.3:c.298G>T	NP_002042.1:p.Gly100Cys