Canonical Allele Identifier: CA375965475

Gene: GATA3

Linked Data

• gnomAD v4: 10-8055830-C-A
• MyVariant Identifiers: chr10:g.8097793C>A (hg19) ; chr10:g.8055830C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8055830C>A , CM000672.2:g.8055830C>A	GRCh38
NC_000010.10:g.8097793C>A , CM000672.1:g.8097793C>A	GRCh37
NC_000010.9:g.8137799C>A	NCBI36
NG_015859.1:g.6127C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.175C>A	ENSP00000341619.3:p.His59Asn
ENST00000379328.9:c.175C>A MANE Select	ENSP00000368632.3:p.His59Asn
ENST00000481743.2:c.175C>A	ENSP00000493486.1:p.His59Asn
ENST00000643001.1:c.175C>A	ENSP00000494284.1:p.His59Asn
ENST00000346208.3:c.175C>A	ENSP00000341619.3:p.His59Asn
ENST00000379328.7:c.175C>A	ENSP00000368632.3:p.His59Asn
NM_001002295.1:c.175C>A	NP_001002295.1:p.His59Asn
NM_002051.2:c.175C>A	NP_002042.1:p.His59Asn
XM_005252442.2:c.175C>A	XP_005252499.1:p.His59Asn
XM_005252443.3:c.175C>A	XP_005252500.1:p.His59Asn
XM_005252443.5:c.175C>A	XP_005252500.1:p.His59Asn
XR_001747358.1:n.617+936G>T
NM_001002295.2:c.175C>A MANE Select	NP_001002295.1:p.His59Asn
NM_002051.3:c.175C>A	NP_002042.1:p.His59Asn