Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475053C= , CM000684.2:g.32475053C= | GRCh38 |
| NC_000022.10:g.32871040C= , CM000684.1:g.32871040C= | GRCh37 |
| NC_000022.9:g.31201040C= | NCBI36 |
| NG_016001.1:g.5334C= | |
| NG_016001.2:g.5334C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.51C= MANE Select | ENSP00000266087.7:p.Pro17= | |
| ENST00000266087.11:c.51C= | ENSP00000266087.7:p.Pro17= | |
| ENST00000420700.5:c.51C= | ENSP00000406155.1:p.Pro17= | |
| ENST00000425028.5:c.51C= | ENSP00000395823.1:p.Pro17= | |
| ENST00000492535.1:n.39C= | ||
| NM_012179.3:c.51C= | NP_036311.3:p.Pro17= | |
| XM_011530106.1:c.-123C= | XP_011528408.1:n.-123C= | |
| XM_024452207.1:c.-140C= | XP_024307975.1:n.-140C= | |
| NM_012179.4:c.51C= MANE Select | NP_036311.3:p.Pro17= |