Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189062878G>T , CM000664.2:g.189062878G>T | GRCh38 |
| NC_000002.11:g.189927604G>T , CM000664.1:g.189927604G>T | GRCh37 |
| NC_000002.10:g.189635849G>T | NCBI36 |
| NG_011799.1:g.122002C>A | |
| NG_011799.2:g.122002C>A | |
| NG_011799.3:g.167424C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.1964C>A MANE Select | ENSP00000364000.3:p.Pro655His | |
| ENST00000374866.7:c.1964C>A | ENSP00000364000.3:p.Pro655His | |
| ENST00000470524.2:n.70C>A | ||
| ENST00000618828.1:c.803C>A | ENSP00000482184.1:p.Pro268His | |
| NM_000393.3:c.1964C>A | NP_000384.2:p.Pro655His | |
| XM_011510573.1:c.1826C>A | XP_011508875.1:p.Pro609His | |
| NM_000393.4:c.1964C>A | NP_000384.2:p.Pro655His | |
| XM_011510573.3:c.1826C>A | XP_011508875.1:p.Pro609His | |
| NM_000393.5:c.1964C>A MANE Select | NP_000384.2:p.Pro655His |