Linked Data
gnomAD v4:
9-841666-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.841666C>T , CM000671.2:g.841666C>T | GRCh38 |
| NC_000009.11:g.841666C>T , CM000671.1:g.841666C>T | GRCh37 |
| NC_000009.10:g.831666C>T | NCBI36 |
| NG_009221.1:g.4977C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_006716732.1:c.-173C>T | XP_006716795.1:n.-173C>T | |
| XM_017014375.1:c.-173C>T | XP_016869864.1:n.-173C>T |