Canonical Allele Identifier: CA375966808
Gene: GATA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 426453
ClinVar RCV Id: RCV000490094
dbSNP Id: rs1085307633
MyVariant Identifiers: chr10:g.8100267G>C (hg19) chr10:g.8058304G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8058304G>C , CM000672.2:g.8058304G>C GRCh38
NC_000010.10:g.8100267G>C , CM000672.1:g.8100267G>C GRCh37
NC_000010.9:g.8140273G>C NCBI36
NG_015859.1:g.8601G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000346208.4:c.242-1G>C ENSP00000341619.3:n.242-1G>C
ENST00000379328.9:c.242-1G>C MANE Select ENSP00000368632.3:n.242-1G>C
ENST00000481743.2:c.242-1G>C ENSP00000493486.1:n.242-1G>C
ENST00000346208.3:c.242-1G>C ENSP00000341619.3:n.242-1G>C
ENST00000379328.7:c.242-1G>C ENSP00000368632.3:n.242-1G>C
NM_001002295.1:c.242-1G>C NP_001002295.1:n.242-1G>C
NM_002051.2:c.242-1G>C NP_002042.1:n.242-1G>C
XM_005252442.2:c.242-1G>C XP_005252499.1:n.242-1G>C
XM_005252443.3:c.242-1G>C XP_005252500.1:n.242-1G>C
XM_005252443.5:c.242-1G>C XP_005252500.1:n.242-1G>C
NM_001002295.2:c.242-1G>C MANE Select NP_001002295.1:n.242-1G>C
NM_002051.3:c.242-1G>C NP_002042.1:n.242-1G>C
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