Linked Data
gnomAD v4:
17-82727693-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82727693C>A , CM000679.2:g.82727693C>A | GRCh38 |
| NC_000017.10:g.80685569C>A , CM000679.1:g.80685569C>A | GRCh37 |
| NC_000017.9:g.78278858C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269373.11:c.*522C>A MANE Select | ENSP00000269373.6:n.*522C>A | |
| ENST00000269373.10:c.*522C>A | ENSP00000269373.6:n.*522C>A | |
| ENST00000571594.1:c.53+526C>A | ENSP00000459751.1:n.53+526C>A | |
| NM_024619.3:c.*522C>A | NP_078895.2:n.*522C>A | |
| NR_046408.1:n.1630C>A | ||
| XM_024450948.1:c.*522C>A | XP_024306716.1:n.*522C>A | |
| NM_024619.4:c.*522C>A MANE Select | NP_078895.2:n.*522C>A | |
| NR_046408.2:n.1630C>A |