Canonical Allele Identifier: CA202464219

Gene: GATA3

Linked Data

• ClinVar Variation Id: 2635669
• ClinVar RCV Id: RCV003427965
• dbSNP Id: rs1025624628
• gnomAD v4: 10-8073771-C-T
• MyVariant Identifiers: chr10:g.8115734C>T (hg19) ; chr10:g.8073771C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073771C>T , CM000672.2:g.8073771C>T	GRCh38
NC_000010.10:g.8115734C>T , CM000672.1:g.8115734C>T	GRCh37
NC_000010.9:g.8155740C>T	NCBI36
NG_015859.1:g.24068C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1080C>T	ENSP00000341619.3:p.Gly360=
ENST00000379328.9:c.1083C>T MANE Select	ENSP00000368632.3:p.Gly361=
ENST00000346208.3:c.1080C>T	ENSP00000341619.3:p.Gly360=
ENST00000379328.7:c.1083C>T	ENSP00000368632.3:p.Gly361=
ENST00000461472.1:n.602C>T
NM_001002295.1:c.1083C>T	NP_001002295.1:p.Gly361=
NM_002051.2:c.1080C>T	NP_002042.1:p.Gly360=
XM_005252442.2:c.1083C>T	XP_005252499.1:p.Gly361=
XM_005252443.3:c.1083C>T	XP_005252500.1:p.Gly361=
XM_005252443.5:c.1083C>T	XP_005252500.1:p.Gly361=
NM_001002295.2:c.1083C>T MANE Select	NP_001002295.1:p.Gly361=
NM_002051.3:c.1080C>T	NP_002042.1:p.Gly360=