Linked Data
gnomAD v4:
15-48410779-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48410779C>A , CM000677.2:g.48410779C>A | GRCh38 |
| NC_000015.9:g.48702976C>A , CM000677.1:g.48702976C>A | GRCh37 |
| NC_000015.8:g.46490268C>A | NCBI36 |
| NG_008805.2:g.240010G>T , LRG_778:g.240010G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1635G>T | ENSP00000453958.2:n.*1635G>T | |
| ENST00000682158.1:n.2208G>T | ||
| ENST00000682170.1:n.3008G>T | ||
| ENST00000682767.1:n.2124G>T | ||
| ENST00000316623.10:c.*211G>T MANE Select | ENSP00000325527.5:n.*211G>T | |
| ENST00000316623.9:c.*211G>T | ENSP00000325527.5:n.*211G>T | |
| ENST00000559133.5:c.4196G>T | ||
| NM_000138.4:c.*211G>T , LRG_778t1:c.*211G>T | NP_000129.3:n.*211G>T | |
| NM_000138.5:c.*211G>T MANE Select | NP_000129.3:n.*211G>T |