Canonical Allele Identifier: CA468400696
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs201916439
MyVariant Identifiers: chr10:g.8115719T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8073756T>C , CM000672.2:g.8073756T>C GRCh38
NC_000010.10:g.8115719T>C , CM000672.1:g.8115719T>C GRCh37
NC_000010.9:g.8155725T>C NCBI36
NG_015859.1:g.24053T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000346208.4:c.1065T>C ENSP00000341619.3:p.Thr355=
ENST00000379328.9:c.1068T>C MANE Select ENSP00000368632.3:p.Thr356=
ENST00000346208.3:c.1065T>C ENSP00000341619.3:p.Thr355=
ENST00000379328.7:c.1068T>C ENSP00000368632.3:p.Thr356=
ENST00000461472.1:n.587T>C
NM_001002295.1:c.1068T>C NP_001002295.1:p.Thr356=
NM_002051.2:c.1065T>C NP_002042.1:p.Thr355=
XM_005252442.2:c.1068T>C XP_005252499.1:p.Thr356=
XM_005252443.3:c.1068T>C XP_005252500.1:p.Thr356=
XM_005252443.5:c.1068T>C XP_005252500.1:p.Thr356=
NM_001002295.2:c.1068T>C MANE Select NP_001002295.1:p.Thr356=
NM_002051.3:c.1065T>C NP_002042.1:p.Thr355=