Linked Data
gnomAD v4:
13-48045829-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045829A>G , CM000675.2:g.48045829A>G | GRCh38 |
| NC_000013.10:g.48619965A>G , CM000675.1:g.48619965A>G | GRCh37 |
| NC_000013.9:g.47517966A>G | NCBI36 |
| NG_047021.1:g.13263A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.*30A>G MANE Select | ENSP00000258662.1:n.*30A>G | |
| ENST00000258662.2:c.*30A>G | ENSP00000258662.1:n.*30A>G | |
| NM_018283.2:c.*30A>G | NP_060753.1:n.*30A>G | |
| NM_018283.3:c.*30A>G | NP_060753.1:n.*30A>G | |
| NR_136687.1:n.705A>G | ||
| NR_136688.1:n.675+30A>G | ||
| NM_018283.4:c.*30A>G MANE Select | NP_060753.1:n.*30A>G | |
| NR_136687.2:n.546A>G | ||
| NR_136688.2:n.516+30A>G |