Canonical Allele Identifier: CA1889018696
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs3824662

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8062245C>G , CM000672.2:g.8062245C>G GRCh38
NC_000010.10:g.8104208C>G , CM000672.1:g.8104208C>G GRCh37
NC_000010.9:g.8144214C>G NCBI36
NG_015859.1:g.12542C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000346208.4:c.779-1751C>G ENSP00000341619.3:n.779-1751C>G
ENST00000379328.9:c.779-1748C>G MANE Select ENSP00000368632.3:n.779-1748C>G
ENST00000346208.3:c.779-1751C>G ENSP00000341619.3:n.779-1751C>G
ENST00000379328.7:c.779-1748C>G ENSP00000368632.3:n.779-1748C>G
ENST00000461472.1:n.443+3404C>G
NM_001002295.1:c.779-1748C>G NP_001002295.1:n.779-1748C>G
NM_002051.2:c.779-1751C>G NP_002042.1:n.779-1751C>G
XM_005252442.2:c.779-1748C>G XP_005252499.1:n.779-1748C>G
XM_005252443.3:c.779-1748C>G XP_005252500.1:n.779-1748C>G
XM_005252443.5:c.779-1748C>G XP_005252500.1:n.779-1748C>G
NM_001002295.2:c.779-1748C>G MANE Select NP_001002295.1:n.779-1748C>G
NM_002051.3:c.779-1751C>G NP_002042.1:n.779-1751C>G