Linked Data
gnomAD v4:
15-74750277-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750277T>G , CM000677.2:g.74750277T>G | GRCh38 |
| NC_000015.9:g.75042618T>G , CM000677.1:g.75042618T>G | GRCh37 |
| NC_000015.8:g.72829671T>G | NCBI36 |
| NG_008431.1:g.32736T>G | |
| NG_008431.2:g.32736T>G | |
| NG_061543.1:g.6433T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.539T>G MANE Select | ENSP00000342007.4:p.Met180Arg | |
| ENST00000343932.4:c.539T>G | ENSP00000342007.4:p.Met180Arg | |
| NM_000761.4:c.539T>G | NP_000752.2:p.Met180Arg | |
| NM_000761.5:c.539T>G MANE Select | NP_000752.2:p.Met180Arg |