Linked Data
gnomAD v4:
15-48520890-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48520890G>T , CM000677.2:g.48520890G>T | GRCh38 |
| NC_000015.9:g.48813087G>T , CM000677.1:g.48813087G>T | GRCh37 |
| NC_000015.8:g.46600379G>T | NCBI36 |
| NG_008805.2:g.129899C>A , LRG_778:g.129899C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.989-73C>A | ENSP00000453958.2:n.989-73C>A | |
| ENST00000674301.2:c.989-73C>A | ENSP00000501333.2:n.989-73C>A | |
| ENST00000316623.10:c.989-73C>A MANE Select | ENSP00000325527.5:n.989-73C>A | |
| ENST00000316623.9:c.989-73C>A | ENSP00000325527.5:n.989-73C>A | |
| ENST00000537463.6:c.636+16821C>A | ENSP00000440294.2:n.636+16821C>A | |
| NM_000138.4:c.989-73C>A , LRG_778t1:c.989-73C>A | NP_000129.3:n.989-73C>A | |
| NM_000138.5:c.989-73C>A MANE Select | NP_000129.3:n.989-73C>A |