Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15879364G>T , CM000681.2:g.15879364G>T | GRCh38 |
| NC_000019.9:g.15990174G>T , CM000681.1:g.15990174G>T | GRCh37 |
| NC_000019.8:g.15851174G>T | NCBI36 |
| NG_007971.2:g.23711C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.1379C>A MANE Select | ENSP00000221700.3:p.Pro460His | |
| ENST00000011989.11:c.1379C>A | ENSP00000011989.8:p.Pro460His | |
| ENST00000221700.10:c.1379C>A | ENSP00000221700.3:p.Pro460His | |
| ENST00000392846.7:n.1322C>A | ||
| ENST00000589654.2:c.167C>A | ||
| NM_001082.4:c.1379C>A | NP_001073.3:p.Pro460His | |
| NM_001082.5:c.1379C>A MANE Select | NP_001073.3:p.Pro460His |