Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149926385G>T , CM000663.2:g.149926385G>T | GRCh38 |
| NC_000001.10:g.149898277G>T , CM000663.1:g.149898277G>T | GRCh37 |
| NC_000001.9:g.148164901G>T | NCBI36 |
| NG_032777.1:g.6868C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.697C>A MANE Select | ENSP00000271628.8:p.Pro233Thr | |
| ENST00000271628.8:c.697C>A | ENSP00000271628.8:p.Pro233Thr | |
| ENST00000457312.1:c.568C>A | ENSP00000391114.1:p.Pro190Thr | |
| NM_005850.4:c.697C>A | NP_005841.1:p.Pro233Thr | |
| NM_005850.5:c.697C>A MANE Select | NP_005841.1:p.Pro233Thr |