Linked Data
gnomAD v4:
12-9116237-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.9116237T>C , CM000674.2:g.9116237T>C | GRCh38 |
| NC_000012.11:g.9268833T>C , CM000674.1:g.9268833T>C | GRCh37 |
| NC_000012.10:g.9160100T>C | NCBI36 |
| NG_011717.1:g.4726A>G | |
| NG_011717.2:g.4726A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017018683.1:c.*34-9137T>C | XP_016874172.1:n.*34-9137T>C | |
| XM_017018684.1:c.*34-18849T>C | XP_016874173.1:n.*34-18849T>C | |
| XM_017018685.1:c.*33+58071T>C | XP_016874174.1:n.*33+58071T>C |