Canonical Allele Identifier: CA468199797
Gene: GATA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.8100689C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8058726C>T , CM000672.2:g.8058726C>T GRCh38
NC_000010.10:g.8100689C>T , CM000672.1:g.8100689C>T GRCh37
NC_000010.9:g.8140695C>T NCBI36
NG_015859.1:g.9023C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.663C>T ENSP00000341619.3:p.Thr221=
ENST00000379328.9:c.663C>T MANE Select ENSP00000368632.3:p.Thr221=
ENST00000346208.3:c.663C>T ENSP00000341619.3:p.Thr221=
ENST00000379328.7:c.663C>T ENSP00000368632.3:p.Thr221=
ENST00000461472.1:n.328C>T
NM_001002295.1:c.663C>T NP_001002295.1:p.Thr221=
NM_002051.2:c.663C>T NP_002042.1:p.Thr221=
XM_005252442.2:c.663C>T XP_005252499.1:p.Thr221=
XM_005252443.3:c.663C>T XP_005252500.1:p.Thr221=
XM_005252443.5:c.663C>T XP_005252500.1:p.Thr221=
NM_001002295.2:c.663C>T MANE Select NP_001002295.1:p.Thr221=
NM_002051.3:c.663C>T NP_002042.1:p.Thr221=