Linked Data
gnomAD v4:
17-8159312-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8159312C>T , CM000679.2:g.8159312C>T | GRCh38 |
| NC_000017.10:g.8062630C>T , CM000679.1:g.8062630C>T | GRCh37 |
| NC_000017.9:g.8003355C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316509.11:c.*1543G>A MANE Select | ENSP00000314214.6:n.*1543G>A | |
| ENST00000316509.10:c.*1543G>A | ENSP00000314214.6:n.*1543G>A | |
| ENST00000498285.1:c.334+2161G>A | ENSP00000464383.1:n.334+2161G>A | |
| NM_014232.2:c.*1543G>A | NP_055047.2:n.*1543G>A | |
| XM_005256775.3:c.*1543G>A | XP_005256832.1:n.*1543G>A | |
| NM_001330125.1:c.*1543G>A | NP_001317054.1:n.*1543G>A | |
| NM_014232.3:c.*1543G>A MANE Select | NP_055047.2:n.*1543G>A |