Linked Data
gnomAD v4:
16-177028-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177028C>A , CM000678.2:g.177028C>A | GRCh38 |
| NC_000016.9:g.227027C>A , CM000678.1:g.227027C>A | GRCh37 |
| NC_000016.8:g.167027C>A | NCBI36 |
| NG_000006.1:g.37891C>A | |
| NG_059186.1:g.5378C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.195C>A MANE Select | ENSP00000322421.5:p.Asp65Glu | |
| ENST00000397797.1:c.99C>A | ENSP00000380899.1:p.Asp33Glu | |
| ENST00000472694.1:n.331C>A | ||
| ENST00000487791.1:n.164C>A | ||
| NM_000558.4:c.195C>A | NP_000549.1:p.Asp65Glu | |
| NM_000558.5:c.195C>A MANE Select | NP_000549.1:p.Asp65Glu |