Linked Data
gnomAD v4:
15-48520898-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48520898A>C , CM000677.2:g.48520898A>C | GRCh38 |
| NC_000015.9:g.48813095A>C , CM000677.1:g.48813095A>C | GRCh37 |
| NC_000015.8:g.46600387A>C | NCBI36 |
| NG_008805.2:g.129891T>G , LRG_778:g.129891T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.989-81T>G | ENSP00000453958.2:n.989-81T>G | |
| ENST00000674301.2:c.989-81T>G | ENSP00000501333.2:n.989-81T>G | |
| ENST00000316623.10:c.989-81T>G MANE Select | ENSP00000325527.5:n.989-81T>G | |
| ENST00000316623.9:c.989-81T>G | ENSP00000325527.5:n.989-81T>G | |
| ENST00000537463.6:c.636+16813T>G | ENSP00000440294.2:n.636+16813T>G | |
| NM_000138.4:c.989-81T>G , LRG_778t1:c.989-81T>G | NP_000129.3:n.989-81T>G | |
| NM_000138.5:c.989-81T>G MANE Select | NP_000129.3:n.989-81T>G |