Linked Data
gnomAD v4:
11-102798292-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798292C>A , CM000673.2:g.102798292C>A | GRCh38 |
| NC_000011.9:g.102669023C>A , CM000673.1:g.102669023C>A | GRCh37 |
| NC_000011.8:g.102174233C>A | NCBI36 |
| NG_011740.1:g.4944G>T | |
| NG_011740.2:g.4944G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371455.7:n.423+170C>A | ||
| ENST00000525739.6:n.682+170C>A | ||
| ENST00000544704.1:n.443+170C>A | ||
| NR_038390.1:n.682+170C>A |