Canonical Allele Identifier: CA5404584
Gene: GATA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2918372
ClinVar RCV Id: RCV003738022
dbSNP Id: rs182422967
ExAC: 10:8115926 G / A
gnomAD v2: 10-8115926-G-A
gnomAD v3: 10-8073963-G-A
gnomAD v4: 10-8073963-G-A
MyVariant Identifiers: chr10:g.8115926G>A (hg19) chr10:g.8073963G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073963G>A , CM000672.2:g.8073963G>A GRCh38
NC_000010.10:g.8115926G>A , CM000672.1:g.8115926G>A GRCh37
NC_000010.9:g.8155932G>A NCBI36
NG_015859.1:g.24260G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.1272G>A ENSP00000341619.3:p.Pro424=
ENST00000379328.9:c.1275G>A MANE Select ENSP00000368632.3:p.Pro425=
ENST00000346208.3:c.1272G>A ENSP00000341619.3:p.Pro424=
ENST00000379328.7:c.1275G>A ENSP00000368632.3:p.Pro425=
ENST00000461472.1:n.794G>A
NM_001002295.1:c.1275G>A NP_001002295.1:p.Pro425=
NM_002051.2:c.1272G>A NP_002042.1:p.Pro424=
XM_005252442.2:c.1275G>A XP_005252499.1:p.Pro425=
XM_005252443.3:c.1275G>A XP_005252500.1:p.Pro425=
XM_005252443.5:c.1275G>A XP_005252500.1:p.Pro425=
NM_001002295.2:c.1275G>A MANE Select NP_001002295.1:p.Pro425=
NM_002051.3:c.1272G>A NP_002042.1:p.Pro424=
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