Canonical Allele Identifier: CA468400832

Gene: GATA3

Linked Data

• dbSNP Id: rs764256467
• gnomAD v2: 10-8100551-G-A
• gnomAD v3: 10-8058588-G-A
• gnomAD v4: 10-8058588-G-A
• COSMIC: COSM81208
• MyVariant Identifiers: chr10:g.8100551G>A (hg19) ; chr10:g.8058588G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058588G>A , CM000672.2:g.8058588G>A	GRCh38
NC_000010.10:g.8100551G>A , CM000672.1:g.8100551G>A	GRCh37
NC_000010.9:g.8140557G>A	NCBI36
NG_015859.1:g.8885G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.525G>A	ENSP00000341619.3:p.Ser175=
ENST00000379328.9:c.525G>A MANE Select	ENSP00000368632.3:p.Ser175=
ENST00000346208.3:c.525G>A	ENSP00000341619.3:p.Ser175=
ENST00000379328.7:c.525G>A	ENSP00000368632.3:p.Ser175=
ENST00000461472.1:n.190G>A
NM_001002295.1:c.525G>A	NP_001002295.1:p.Ser175=
NM_002051.2:c.525G>A	NP_002042.1:p.Ser175=
XM_005252442.2:c.525G>A	XP_005252499.1:p.Ser175=
XM_005252443.3:c.525G>A	XP_005252500.1:p.Ser175=
XM_005252443.5:c.525G>A	XP_005252500.1:p.Ser175=
NM_001002295.2:c.525G>A MANE Select	NP_001002295.1:p.Ser175=
NM_002051.3:c.525G>A	NP_002042.1:p.Ser175=