Canonical Allele Identifier: CA202464074

Gene: GATA3

Linked Data

• dbSNP Id: rs890038716
• gnomAD v2: 10-8115658-A-G
• gnomAD v4: 10-8073695-A-G
• MyVariant Identifiers: chr10:g.8115658A>G (hg19) ; chr10:g.8073695A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073695A>G , CM000672.2:g.8073695A>G	GRCh38
NC_000010.10:g.8115658A>G , CM000672.1:g.8115658A>G	GRCh37
NC_000010.9:g.8155664A>G	NCBI36
NG_015859.1:g.23992A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000346208.4:c.1048-44A>G	ENSP00000341619.3:n.1048-44A>G
ENST00000379328.9:c.1051-44A>G MANE Select	ENSP00000368632.3:n.1051-44A>G
ENST00000346208.3:c.1048-44A>G	ENSP00000341619.3:n.1048-44A>G
ENST00000379328.7:c.1051-44A>G	ENSP00000368632.3:n.1051-44A>G
ENST00000461472.1:n.570-44A>G
NM_001002295.1:c.1051-44A>G	NP_001002295.1:n.1051-44A>G
NM_002051.2:c.1048-44A>G	NP_002042.1:n.1048-44A>G
XM_005252442.2:c.1051-44A>G	XP_005252499.1:n.1051-44A>G
XM_005252443.3:c.1051-44A>G	XP_005252500.1:n.1051-44A>G
XM_005252443.5:c.1051-44A>G	XP_005252500.1:n.1051-44A>G
NM_001002295.2:c.1051-44A>G MANE Select	NP_001002295.1:n.1051-44A>G
NM_002051.3:c.1048-44A>G	NP_002042.1:n.1048-44A>G