Canonical Allele Identifier: CA375966915

Gene: GATA3

Linked Data

• dbSNP Id: rs2131488310
• MyVariant Identifiers: chr10:g.8100319A>T (hg19) ; chr10:g.8058356A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8058356A>T , CM000672.2:g.8058356A>T	GRCh38
NC_000010.10:g.8100319A>T , CM000672.1:g.8100319A>T	GRCh37
NC_000010.9:g.8140325A>T	NCBI36
NG_015859.1:g.8653A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346208.4:c.293A>T	ENSP00000341619.3:p.Asp98Val
ENST00000379328.9:c.293A>T MANE Select	ENSP00000368632.3:p.Asp98Val
ENST00000481743.2:c.293A>T	ENSP00000493486.1:p.Asp98Val
ENST00000346208.3:c.293A>T	ENSP00000341619.3:p.Asp98Val
ENST00000379328.7:c.293A>T	ENSP00000368632.3:p.Asp98Val
NM_001002295.1:c.293A>T	NP_001002295.1:p.Asp98Val
NM_002051.2:c.293A>T	NP_002042.1:p.Asp98Val
XM_005252442.2:c.293A>T	XP_005252499.1:p.Asp98Val
XM_005252443.3:c.293A>T	XP_005252500.1:p.Asp98Val
XM_005252443.5:c.293A>T	XP_005252500.1:p.Asp98Val
NM_001002295.2:c.293A>T MANE Select	NP_001002295.1:p.Asp98Val
NM_002051.3:c.293A>T	NP_002042.1:p.Asp98Val