Linked Data
gnomAD v4:
12-9116261-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.9116261C>A , CM000674.2:g.9116261C>A | GRCh38 |
| NC_000012.11:g.9268857C>A , CM000674.1:g.9268857C>A | GRCh37 |
| NC_000012.10:g.9160124C>A | NCBI36 |
| NG_011717.1:g.4702G>T | |
| NG_011717.2:g.4702G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017018683.1:c.*34-9113C>A | XP_016874172.1:n.*34-9113C>A | |
| XM_017018684.1:c.*34-18825C>A | XP_016874173.1:n.*34-18825C>A | |
| XM_017018685.1:c.*33+58095C>A | XP_016874174.1:n.*33+58095C>A |