Linked Data
gnomAD v4:
15-48410627-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48410627T>C , CM000677.2:g.48410627T>C | GRCh38 |
| NC_000015.9:g.48702824T>C , CM000677.1:g.48702824T>C | GRCh37 |
| NC_000015.8:g.46490116T>C | NCBI36 |
| NG_008805.2:g.240162A>G , LRG_778:g.240162A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1787A>G | ENSP00000453958.2:n.*1787A>G | |
| ENST00000682158.1:n.2360A>G | ||
| ENST00000682170.1:n.3160A>G | ||
| ENST00000682767.1:n.2276A>G | ||
| ENST00000316623.10:c.*363A>G MANE Select | ENSP00000325527.5:n.*363A>G | |
| ENST00000316623.9:c.*363A>G | ENSP00000325527.5:n.*363A>G | |
| ENST00000559133.5:c.4348A>G | ||
| NM_000138.4:c.*363A>G , LRG_778t1:c.*363A>G | NP_000129.3:n.*363A>G | |
| NM_000138.5:c.*363A>G MANE Select | NP_000129.3:n.*363A>G |