Canonical Allele Identifier: CA468400538
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs1832681845
gnomAD v4: 10-8058423-G-A
MyVariant Identifiers: chr10:g.8100386G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8058423G>A , CM000672.2:g.8058423G>A GRCh38
NC_000010.10:g.8100386G>A , CM000672.1:g.8100386G>A GRCh37
NC_000010.9:g.8140392G>A NCBI36
NG_015859.1:g.8720G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.360G>A ENSP00000341619.3:p.Thr120=
ENST00000379328.9:c.360G>A MANE Select ENSP00000368632.3:p.Thr120=
ENST00000481743.2:c.360G>A ENSP00000493486.1:p.Thr120=
ENST00000346208.3:c.360G>A ENSP00000341619.3:p.Thr120=
ENST00000379328.7:c.360G>A ENSP00000368632.3:p.Thr120=
ENST00000461472.1:n.25G>A
NM_001002295.1:c.360G>A NP_001002295.1:p.Thr120=
NM_002051.2:c.360G>A NP_002042.1:p.Thr120=
XM_005252442.2:c.360G>A XP_005252499.1:p.Thr120=
XM_005252443.3:c.360G>A XP_005252500.1:p.Thr120=
XM_005252443.5:c.360G>A XP_005252500.1:p.Thr120=
NM_001002295.2:c.360G>A MANE Select NP_001002295.1:p.Thr120=
NM_002051.3:c.360G>A NP_002042.1:p.Thr120=