Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911141G>T , CM000679.2:g.42911141G>T | GRCh38 |
| NC_000017.10:g.41063158G>T , CM000679.1:g.41063158G>T | GRCh37 |
| NC_000017.9:g.38316684G>T | NCBI36 |
| NG_011808.1:g.15344G>T , LRG_147:g.15344G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.789G>T MANE Select | ENSP00000253801.1:p.Lys263Asn | |
| ENST00000253801.6:c.789G>T | ENSP00000253801.1:p.Lys263Asn | |
| ENST00000585489.1:c.*181G>T | ENSP00000466202.1:n.*181G>T | |
| ENST00000592383.5:c.*181G>T | ENSP00000465958.1:n.*181G>T | |
| NM_000151.3:c.789G>T | NP_000142.2:p.Lys263Asn | |
| NM_001270397.1:c.*181G>T | NP_001257326.1:n.*181G>T | |
| NM_000151.4:c.789G>T MANE Select | NP_000142.2:p.Lys263Asn | |
| NM_001270397.2:c.*181G>T | NP_001257326.1:n.*181G>T |