Linked Data
gnomAD v4:
17-8159241-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8159241C>T , CM000679.2:g.8159241C>T | GRCh38 |
| NC_000017.10:g.8062559C>T , CM000679.1:g.8062559C>T | GRCh37 |
| NC_000017.9:g.8003284C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316509.11:c.*1614G>A MANE Select | ENSP00000314214.6:n.*1614G>A | |
| ENST00000316509.10:c.*1614G>A | ENSP00000314214.6:n.*1614G>A | |
| ENST00000498285.1:c.334+2232G>A | ENSP00000464383.1:n.334+2232G>A | |
| NM_014232.2:c.*1614G>A | NP_055047.2:n.*1614G>A | |
| NM_001330125.1:c.*1614G>A | NP_001317054.1:n.*1614G>A | |
| NM_014232.3:c.*1614G>A MANE Select | NP_055047.2:n.*1614G>A |