Linked Data
gnomAD v4:
17-82727698-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82727698T>C , CM000679.2:g.82727698T>C | GRCh38 |
| NC_000017.10:g.80685574T>C , CM000679.1:g.80685574T>C | GRCh37 |
| NC_000017.9:g.78278863T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269373.11:c.*527T>C MANE Select | ENSP00000269373.6:n.*527T>C | |
| ENST00000269373.10:c.*527T>C | ENSP00000269373.6:n.*527T>C | |
| ENST00000571594.1:c.53+531T>C | ENSP00000459751.1:n.53+531T>C | |
| NM_024619.3:c.*527T>C | NP_078895.2:n.*527T>C | |
| NR_046408.1:n.1635T>C | ||
| XM_024450948.1:c.*527T>C | XP_024306716.1:n.*527T>C | |
| NM_024619.4:c.*527T>C MANE Select | NP_078895.2:n.*527T>C | |
| NR_046408.2:n.1635T>C |