Canonical Allele Identifier: CA375970569

Gene: GATA3

Linked Data

• dbSNP Id: rs1564399262
• gnomAD v4: 10-8058754-T-A
• MyVariant Identifiers: chr10:g.8100717T>A (hg19) ; chr10:g.8058754T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058754T>A , CM000672.2:g.8058754T>A	GRCh38
NC_000010.10:g.8100717T>A , CM000672.1:g.8100717T>A	GRCh37
NC_000010.9:g.8140723T>A	NCBI36
NG_015859.1:g.9051T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.691T>A	ENSP00000341619.3:p.Ser231Thr
ENST00000379328.9:c.691T>A MANE Select	ENSP00000368632.3:p.Ser231Thr
ENST00000346208.3:c.691T>A	ENSP00000341619.3:p.Ser231Thr
ENST00000379328.7:c.691T>A	ENSP00000368632.3:p.Ser231Thr
ENST00000461472.1:n.356T>A
NM_001002295.1:c.691T>A	NP_001002295.1:p.Ser231Thr
NM_002051.2:c.691T>A	NP_002042.1:p.Ser231Thr
XM_005252442.2:c.691T>A	XP_005252499.1:p.Ser231Thr
XM_005252443.3:c.691T>A	XP_005252500.1:p.Ser231Thr
XM_005252443.5:c.691T>A	XP_005252500.1:p.Ser231Thr
NM_001002295.2:c.691T>A MANE Select	NP_001002295.1:p.Ser231Thr
NM_002051.3:c.691T>A	NP_002042.1:p.Ser231Thr