Canonical Allele Identifier: CA202455434

Gene: GATA3

Linked Data

• ClinVar Variation Id: 3233839
• ClinVar RCV Id: RCV004527119
• dbSNP Id: rs143582578
• gnomAD v2: 10-8100734-C-G
• gnomAD v3: 10-8058771-C-G
• gnomAD v4: 10-8058771-C-G
• MyVariant Identifiers: chr10:g.8100734C>G (hg19) ; chr10:g.8058771C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058771C>G , CM000672.2:g.8058771C>G	GRCh38
NC_000010.10:g.8100734C>G , CM000672.1:g.8100734C>G	GRCh37
NC_000010.9:g.8140740C>G	NCBI36
NG_015859.1:g.9068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.708C>G	ENSP00000341619.3:p.Pro236=
ENST00000379328.9:c.708C>G MANE Select	ENSP00000368632.3:p.Pro236=
ENST00000346208.3:c.708C>G	ENSP00000341619.3:p.Pro236=
ENST00000379328.7:c.708C>G	ENSP00000368632.3:p.Pro236=
ENST00000461472.1:n.373C>G
NM_001002295.1:c.708C>G	NP_001002295.1:p.Pro236=
NM_002051.2:c.708C>G	NP_002042.1:p.Pro236=
XM_005252442.2:c.708C>G	XP_005252499.1:p.Pro236=
XM_005252443.3:c.708C>G	XP_005252500.1:p.Pro236=
XM_005252443.5:c.708C>G	XP_005252500.1:p.Pro236=
NM_001002295.2:c.708C>G MANE Select	NP_001002295.1:p.Pro236=
NM_002051.3:c.708C>G	NP_002042.1:p.Pro236=