Linked Data
gnomAD v4:
16-173678-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173678C>A , CM000678.2:g.173678C>A | GRCh38 |
| NC_000016.9:g.223677C>A , CM000678.1:g.223677C>A | GRCh37 |
| NC_000016.8:g.163677C>A | NCBI36 |
| NG_000006.1:g.34541C>A | |
| NG_059186.1:g.2028C>A | |
| NG_059271.1:g.5832C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.*78C>A MANE Select | ENSP00000251595.6:n.*78C>A | |
| ENST00000251595.10:c.*78C>A | ENSP00000251595.6:n.*78C>A | |
| ENST00000397806.1:c.*78C>A | ENSP00000380908.1:n.*78C>A | |
| NM_000517.4:c.*78C>A | NP_000508.1:n.*78C>A | |
| NM_000517.6:c.*78C>A MANE Select | NP_000508.1:n.*78C>A |