Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6770355C>A , CM000682.2:g.6770355C>A | GRCh38 |
| NC_000020.10:g.6751002C>A , CM000682.1:g.6751002C>A | GRCh37 |
| NC_000020.9:g.6699002C>A | NCBI36 |
| NG_023233.1:g.7258C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378827.5:c.229C>A MANE Select | ENSP00000368104.3:p.Pro77Thr | |
| ENST00000378827.4:c.229C>A | ENSP00000368104.3:p.Pro77Thr | |
| NM_001200.2:c.229C>A | NP_001191.1:p.Pro77Thr | |
| XM_011529323.1:c.-123+1480C>A | XP_011527625.1:n.-123+1480C>A | |
| NM_001200.3:c.229C>A | NP_001191.1:p.Pro77Thr | |
| NM_001200.4:c.229C>A MANE Select | NP_001191.1:p.Pro77Thr |