Canonical Allele Identifier: CA591844067

Gene: GATA3

Linked Data

• dbSNP Id: rs1163991733
• gnomAD v2: 10-8115655-G-A
• gnomAD v3: 10-8073692-G-A
• gnomAD v4: 10-8073692-G-A
• MyVariant Identifiers: chr10:g.8115655G>A (hg19) ; chr10:g.8073692G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073692G>A , CM000672.2:g.8073692G>A	GRCh38
NC_000010.10:g.8115655G>A , CM000672.1:g.8115655G>A	GRCh37
NC_000010.9:g.8155661G>A	NCBI36
NG_015859.1:g.23989G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346208.4:c.1048-47G>A	ENSP00000341619.3:n.1048-47G>A
ENST00000379328.9:c.1051-47G>A MANE Select	ENSP00000368632.3:n.1051-47G>A
ENST00000346208.3:c.1048-47G>A	ENSP00000341619.3:n.1048-47G>A
ENST00000379328.7:c.1051-47G>A	ENSP00000368632.3:n.1051-47G>A
ENST00000461472.1:n.570-47G>A
NM_001002295.1:c.1051-47G>A	NP_001002295.1:n.1051-47G>A
NM_002051.2:c.1048-47G>A	NP_002042.1:n.1048-47G>A
XM_005252442.2:c.1051-47G>A	XP_005252499.1:n.1051-47G>A
XM_005252443.3:c.1051-47G>A	XP_005252500.1:n.1051-47G>A
XM_005252443.5:c.1051-47G>A	XP_005252500.1:n.1051-47G>A
NM_001002295.2:c.1051-47G>A MANE Select	NP_001002295.1:n.1051-47G>A
NM_002051.3:c.1048-47G>A	NP_002042.1:n.1048-47G>A