Linked Data
gnomAD v4:
10-93601764-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93601764G>T , CM000672.2:g.93601764G>T | GRCh38 |
| NC_000010.10:g.95361521G>T , CM000672.1:g.95361521G>T | GRCh37 |
| NC_000010.9:g.95351511G>T | NCBI36 |
| NG_009104.1:g.4473C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000604414.1:c.697-2310G>T | ENSP00000474477.1:n.697-2310G>T |