Canonical Allele Identifier: CA468200135
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs104894162
MyVariant Identifiers: chr10:g.8106006C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8064043C>A , CM000672.2:g.8064043C>A GRCh38
NC_000010.10:g.8106006C>A , CM000672.1:g.8106006C>A GRCh37
NC_000010.9:g.8146012C>A NCBI36
NG_015859.1:g.14340C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000346208.4:c.826C>A ENSP00000341619.3:p.Arg276=
ENST00000379328.9:c.829C>A MANE Select ENSP00000368632.3:p.Arg277=
ENST00000346208.3:c.826C>A ENSP00000341619.3:p.Arg276=
ENST00000379328.7:c.829C>A ENSP00000368632.3:p.Arg277=
ENST00000461472.1:n.443+5202C>A
NM_001002295.1:c.829C>A NP_001002295.1:p.Arg277=
NM_002051.2:c.826C>A NP_002042.1:p.Arg276=
XM_005252442.2:c.829C>A XP_005252499.1:p.Arg277=
XM_005252443.3:c.829C>A XP_005252500.1:p.Arg277=
XM_005252443.5:c.829C>A XP_005252500.1:p.Arg277=
NM_001002295.2:c.829C>A MANE Select NP_001002295.1:p.Arg277=
NM_002051.3:c.826C>A NP_002042.1:p.Arg276=