Linked Data
gnomAD v4:
1-17018846-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17018846G>T , CM000663.2:g.17018846G>T | GRCh38 |
| NC_000001.10:g.17345341G>T , CM000663.1:g.17345341G>T | GRCh37 |
| NC_000001.9:g.17217928G>T | NCBI36 |
| NG_012340.1:g.40325C>A , LRG_316:g.40325C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463045.3:c.*35C>A | ENSP00000481376.2:n.*35C>A | |
| ENST00000491274.6:c.*35C>A | ENSP00000480482.2:n.*35C>A | |
| ENST00000375499.8:c.*35C>A MANE Select | ENSP00000364649.3:n.*35C>A | |
| ENST00000375499.7:c.*35C>A | ENSP00000364649.3:n.*35C>A | |
| ENST00000475049.5:n.303C>A | ||
| ENST00000485092.5:n.542C>A | ||
| NM_003000.2:c.*35C>A , LRG_316t1:c.*35C>A | NP_002991.2:n.*35C>A | |
| NM_003000.3:c.*35C>A MANE Select | NP_002991.2:n.*35C>A |