Canonical Allele Identifier: CA202464431

Gene: GATA3

Linked Data

• dbSNP Id: rs1044699217
• gnomAD v4: 10-8074027-C-A
• MyVariant Identifiers: chr10:g.8115990C>A (hg19) ; chr10:g.8074027C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8074027C>A , CM000672.2:g.8074027C>A	GRCh38
NC_000010.10:g.8115990C>A , CM000672.1:g.8115990C>A	GRCh37
NC_000010.9:g.8155996C>A	NCBI36
NG_015859.1:g.24324C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.*4C>A	ENSP00000341619.3:n.*4C>A
ENST00000379328.9:c.*4C>A MANE Select	ENSP00000368632.3:n.*4C>A
ENST00000346208.3:c.*4C>A	ENSP00000341619.3:n.*4C>A
ENST00000379328.7:c.*4C>A	ENSP00000368632.3:n.*4C>A
ENST00000461472.1:n.858C>A
NM_001002295.1:c.*4C>A	NP_001002295.1:n.*4C>A
NM_002051.2:c.*4C>A	NP_002042.1:n.*4C>A
XM_005252442.2:c.*4C>A	XP_005252499.1:n.*4C>A
XM_005252443.3:c.*4C>A	XP_005252500.1:n.*4C>A
XM_005252443.5:c.*4C>A	XP_005252500.1:n.*4C>A
NM_001002295.2:c.*4C>A MANE Select	NP_001002295.1:n.*4C>A
NM_002051.3:c.*4C>A	NP_002042.1:n.*4C>A