Linked Data
gnomAD v4:
8-16992994-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16992994G>A , CM000670.2:g.16992994G>A | GRCh38 |
| NC_000008.10:g.16850503G>A , CM000670.1:g.16850503G>A | GRCh37 |
| NC_000008.9:g.16894874G>A | NCBI36 |
| NG_015978.1:g.14172C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*78C>T MANE Select | ENSP00000180166.5:n.*78C>T | |
| ENST00000180166.5:c.*78C>T | ENSP00000180166.5:n.*78C>T | |
| ENST00000519941.1:c.418C>T | ||
| NM_019851.2:c.*78C>T | NP_062825.1:n.*78C>T | |
| NM_019851.3:c.*78C>T MANE Select | NP_062825.1:n.*78C>T |