Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475051C= , CM000684.2:g.32475051C= | GRCh38 |
| NC_000022.10:g.32871038C= , CM000684.1:g.32871038C= | GRCh37 |
| NC_000022.9:g.31201038C= | NCBI36 |
| NG_016001.1:g.5332C= | |
| NG_016001.2:g.5332C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.49C= MANE Select | ENSP00000266087.7:p.Pro17= | |
| ENST00000266087.11:c.49C= | ENSP00000266087.7:p.Pro17= | |
| ENST00000420700.5:c.49C= | ENSP00000406155.1:p.Pro17= | |
| ENST00000425028.5:c.49C= | ENSP00000395823.1:p.Pro17= | |
| ENST00000492535.1:n.37C= | ||
| NM_012179.3:c.49C= | NP_036311.3:p.Pro17= | |
| XM_011530106.1:c.-125C= | XP_011528408.1:n.-125C= | |
| XM_024452207.1:c.-142C= | XP_024307975.1:n.-142C= | |
| NM_012179.4:c.49C= MANE Select | NP_036311.3:p.Pro17= |