Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24259744C>G , CM000676.2:g.24259744C>G | GRCh38 |
| NC_000014.8:g.24728950C>G , CM000676.1:g.24728950C>G | GRCh37 |
| NC_000014.7:g.23798790C>G | NCBI36 |
| NG_007150.1:g.8423G>C | |
| NG_007150.2:g.8423G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000359.3:c.944G>C MANE Select | NP_000350.1:p.Arg315Pro |
| ENST00000206765.11:c.944G>C MANE Select | ENSP00000206765.6:p.Arg315Pro |
| NM_000359.2:c.944G>C | NP_000350.1:p.Arg315Pro |
| ENST00000206765.10:c.944G>C | ENSP00000206765.6:p.Arg315Pro |
| ENST00000544573.5:c.-28-1356G>C | ENSP00000439446.1:n.-28-1356G>C |
| ENST00000559136.1:c.17G>C | ENSP00000453337.1:p.Arg6Pro |