Linked Data
gnomAD v4:
9-841682-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.841682T>C , CM000671.2:g.841682T>C | GRCh38 |
| NC_000009.11:g.841682T>C , CM000671.1:g.841682T>C | GRCh37 |
| NC_000009.10:g.831682T>C | NCBI36 |
| NG_009221.1:g.4993T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_006716732.1:c.-157T>C | XP_006716795.1:n.-157T>C | |
| XM_017014375.1:c.-157T>C | XP_016869864.1:n.-157T>C |