Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10692805G= , CM000679.2:g.10692805G= | GRCh38 |
| NC_000017.10:g.10596122G= , CM000679.1:g.10596122G= | GRCh37 |
| NC_000017.9:g.10536847G= | NCBI36 |
| NG_008228.2:g.9764C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004589.4:c.521C= MANE Select | NP_004580.1:p.Pro174= |
| ENST00000255390.10:c.521C= MANE Select | ENSP00000255390.5:p.Pro174= |
| NM_004589.3:c.521C= | NP_004580.1:p.Pro174= |
| ENST00000255390.9:c.521C= | ENSP00000255390.5:p.Pro174= |
| ENST00000577335.1:c.*248C= | ENSP00000464032.1:n.*248C= |
| ENST00000577335.2:c.*248C= | ENSP00000464032.1:n.*248C= |
| ENST00000577427.1:c.469+52C= | ENSP00000463387.1:n.469+52C= |
| XM_005256751.2:c.188C= | XP_005256808.1:p.Pro63= |
| XM_005256751.4:c.188C= | XP_005256808.1:p.Pro63= |