Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63963718C>G , CM000679.2:g.63963718C>G | GRCh38 |
| NC_000017.10:g.62041078C>G , CM000679.1:g.62041078C>G | GRCh37 |
| NC_000017.9:g.59394810C>G | NCBI36 |
| NG_011699.1:g.14201G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.1560G>C MANE Select | NP_000325.4:p.Pro520= |
| ENST00000435607.3:c.1560G>C MANE Select | ENSP00000396320.1:p.Pro520= |
| ENST00000578147.5:c.1560G>C | ENSP00000463963.1:p.Pro520= |
| XM_005257566.3:c.1560G>C | XP_005257623.1:p.Pro520= |
| XR_001752969.1:n.1327-366C>G | |
| XR_001752970.1:n.279-366C>G | |
| XR_934910.1:n.174+404C>G | |
| XR_934910.2:n.1326+404C>G |