Linked Data
gnomAD v4:
13-28659007-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.28659007G>T , CM000675.2:g.28659007G>T | GRCh38 |
| NC_000013.10:g.29233144G>T , CM000675.1:g.29233144G>T | GRCh37 |
| NC_000013.9:g.28131144G>T | NCBI36 |
| NG_027550.1:g.5004G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_015932.5:c.-178G>T | NP_057016.1:n.-178G>T |