Linked Data
gnomAD v4:
15-40471200-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40471200A>G , CM000677.2:g.40471200A>G | GRCh38 |
| NC_000015.9:g.40763399A>G , CM000677.1:g.40763399A>G | GRCh37 |
| NC_000015.8:g.38550691A>G | NCBI36 |
| NG_017074.1:g.5240A>G , LRG_600:g.5240A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.-14A>G MANE Select | ENSP00000307297.6:n.-14A>G | |
| ENST00000306243.6:c.-14A>G | ENSP00000307297.5:n.-14A>G | |
| ENST00000559991.1:c.-14A>G | ENSP00000453882.1:n.-14A>G | |
| NM_130468.3:c.-14A>G , LRG_600t1:c.-14A>G | NP_569735.1:n.-14A>G | |
| NM_130468.4:c.-14A>G MANE Select | NP_569735.1:n.-14A>G |