MyVariant.info:
GRCh37
chr10:g.8093034G>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.8051071G>C , CM000672.2:g.8051071G>C | GRCh38 |
| NC_000010.10:g.8093034G>C , CM000672.1:g.8093034G>C | GRCh37 |
| NC_000010.9:g.8133040G>C | NCBI36 |
| NG_015859.1:g.1368G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643001.1:c.-369-4216G>C (GATA3) | ENSP00000494284.1:n.-369-4216G>C | |
| NR_024256.1:n.1593C>G (GATA3-AS1) | ||
| NR_104328.1:n.401+203C>G (GATA3-AS1) | ||
| NR_104329.1:n.543+110C>G (GATA3-AS1) | ||
| NR_104330.1:n.426+178C>G (GATA3-AS1) | ||
| XM_005252443.3:c.-369-4216G>C (GATA3) | XP_005252500.1:n.-369-4216G>C | |
| XM_005252443.5:c.-369-4216G>C (GATA3) | XP_005252500.1:n.-369-4216G>C |