Linked Data
gnomAD v4:
14-24255993-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24255993G>A , CM000676.2:g.24255993G>A | GRCh38 |
| NC_000014.8:g.24725199G>A , CM000676.1:g.24725199G>A | GRCh37 |
| NC_000014.7:g.23795039G>A | NCBI36 |
| NG_007150.1:g.12174C>T | |
| NG_007150.2:g.12174C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206765.11:c.1487C>T MANE Select | ENSP00000206765.6:p.Ala496Val | |
| ENST00000206765.10:c.1487C>T | ENSP00000206765.6:p.Ala496Val | |
| ENST00000544573.5:c.161C>T | ENSP00000439446.1:p.Ala54Val | |
| ENST00000559136.1:c.560C>T | ENSP00000453337.1:p.Ala187Val | |
| NM_000359.2:c.1487C>T | NP_000350.1:p.Ala496Val | |
| NM_000359.3:c.1487C>T MANE Select | NP_000350.1:p.Ala496Val |