Canonical Allele Identifier: CA924691932

Gene: GATA3

Linked Data

• dbSNP Id: rs1832965383
• gnomAD v3: 10-8073607-G-A
• gnomAD v4: 10-8073607-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073607G>A , CM000672.2:g.8073607G>A	GRCh38
NC_000010.10:g.8115570G>A , CM000672.1:g.8115570G>A	GRCh37
NC_000010.9:g.8155576G>A	NCBI36
NG_015859.1:g.23904G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346208.4:c.1048-132G>A	ENSP00000341619.3:n.1048-132G>A
ENST00000379328.9:c.1051-132G>A MANE Select	ENSP00000368632.3:n.1051-132G>A
ENST00000346208.3:c.1048-132G>A	ENSP00000341619.3:n.1048-132G>A
ENST00000379328.7:c.1051-132G>A	ENSP00000368632.3:n.1051-132G>A
ENST00000461472.1:n.570-132G>A
NM_001002295.1:c.1051-132G>A	NP_001002295.1:n.1051-132G>A
NM_002051.2:c.1048-132G>A	NP_002042.1:n.1048-132G>A
XM_005252442.2:c.1051-132G>A	XP_005252499.1:n.1051-132G>A
XM_005252443.3:c.1051-132G>A	XP_005252500.1:n.1051-132G>A
XM_005252443.5:c.1051-132G>A	XP_005252500.1:n.1051-132G>A
NM_001002295.2:c.1051-132G>A MANE Select	NP_001002295.1:n.1051-132G>A
NM_002051.3:c.1048-132G>A	NP_002042.1:n.1048-132G>A