Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48307305C>A , CM000675.2:g.48307305C>A | GRCh38 |
| NC_000013.10:g.48881441C>A , CM000675.1:g.48881441C>A | GRCh37 |
| NC_000013.9:g.47779442C>A | NCBI36 |
| NG_009009.1:g.8559C>A , LRG_517:g.8559C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.163C>A MANE Select | NP_000312.2:p.Pro55Thr |
| ENST00000267163.6:c.163C>A MANE Select | ENSP00000267163.4:p.Pro55Thr |
| NM_000321.2:c.163C>A , LRG_517t1:c.163C>A | NP_000312.2:p.Pro55Thr |
| ENST00000267163.4:c.163C>A | ENSP00000267163.4:p.Pro55Thr |
| ENST00000467505.5:c.137+3256C>A | ENSP00000434702.1:n.137+3256C>A |
| ENST00000525036.1:n.325C>A | |
| ENST00000646097.1:c.163C>A | ENSP00000496556.1:p.Pro55Thr |
| ENST00000650461.1:c.163C>A | ENSP00000497193.1:p.Pro55Thr |