Canonical Allele Identifier: CA591844075

Gene: GATA3

Linked Data

• dbSNP Id: rs1285678114
• gnomAD v2: 10-8115672-A-G
• MyVariant Identifiers: chr10:g.8115672A>G (hg19) ; chr10:g.8073709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8073709A>G , CM000672.2:g.8073709A>G	GRCh38
NC_000010.10:g.8115672A>G , CM000672.1:g.8115672A>G	GRCh37
NC_000010.9:g.8155678A>G	NCBI36
NG_015859.1:g.24006A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.1048-30A>G	ENSP00000341619.3:n.1048-30A>G
ENST00000379328.9:c.1051-30A>G MANE Select	ENSP00000368632.3:n.1051-30A>G
ENST00000346208.3:c.1048-30A>G	ENSP00000341619.3:n.1048-30A>G
ENST00000379328.7:c.1051-30A>G	ENSP00000368632.3:n.1051-30A>G
ENST00000461472.1:n.570-30A>G
NM_001002295.1:c.1051-30A>G	NP_001002295.1:n.1051-30A>G
NM_002051.2:c.1048-30A>G	NP_002042.1:n.1048-30A>G
XM_005252442.2:c.1051-30A>G	XP_005252499.1:n.1051-30A>G
XM_005252443.3:c.1051-30A>G	XP_005252500.1:n.1051-30A>G
XM_005252443.5:c.1051-30A>G	XP_005252500.1:n.1051-30A>G
NM_001002295.2:c.1051-30A>G MANE Select	NP_001002295.1:n.1051-30A>G
NM_002051.3:c.1048-30A>G	NP_002042.1:n.1048-30A>G