Linked Data
gnomAD v4:
17-47744727-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47744727T>C , CM000679.2:g.47744727T>C | GRCh38 |
| NC_000017.10:g.45822093T>C , CM000679.1:g.45822093T>C | GRCh37 |
| NC_000017.9:g.43177092T>C | NCBI36 |
| NG_012166.1:g.16484T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.990-21T>C MANE Select | ENSP00000177694.1:n.990-21T>C | |
| ENST00000177694.1:c.990-21T>C | ENSP00000177694.1:n.990-21T>C | |
| NM_013351.1:c.990-21T>C | NP_037483.1:n.990-21T>C | |
| XM_011524698.1:c.1053-21T>C | XP_011523000.1:n.1053-21T>C | |
| XM_011524699.1:c.657-21T>C | XP_011523001.1:n.657-21T>C | |
| NM_013351.2:c.990-21T>C MANE Select | NP_037483.1:n.990-21T>C |