Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114674369G>A , CM000674.2:g.114674369G>A | GRCh38 |
| NC_000012.11:g.115112174G>A , CM000674.1:g.115112174G>A | GRCh37 |
| NC_000012.10:g.113596557G>A | NCBI36 |
| NG_008315.1:g.14796C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005996.4:c.1506C>T MANE Select | NP_005987.3:p.Pro502= |
| ENST00000349155.7:c.1506C>T MANE Select | ENSP00000257567.2:p.Pro502= |
| NM_005996.3:c.1506C>T | NP_005987.3:p.Pro502= |
| NM_016569.3:c.1566C>T | NP_057653.3:p.Pro522= |
| NM_016569.4:c.1566C>T | NP_057653.3:p.Pro522= |
| ENST00000257566.7:c.1566C>T | ENSP00000257566.3:p.Pro522= |
| ENST00000349155.6:c.1506C>T | ENSP00000257567.2:p.Pro502= |
| ENST00000613550.1:c.1506C>T | ENSP00000480048.1:p.Pro502= |