Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401394C= , CM000685.2:g.38401394C= | GRCh38 |
| NC_000023.10:g.38260647C= , CM000685.1:g.38260647C= | GRCh37 |
| NC_000023.9:g.38145591C= | NCBI36 |
| NG_008471.1:g.53912C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.506C= MANE Select | ENSP00000039007.4:p.Pro169= | |
| ENST00000643344.1:c.*256C= | ENSP00000496606.1:n.*256C= | |
| ENST00000039007.4:c.506C= | ENSP00000039007.4:p.Pro169= | |
| ENST00000465127.1:c.172-264727C= | ENSP00000417050.1:n.172-264727C= | |
| ENST00000488812.1:n.543C= | ||
| NM_000531.5:c.506C= | NP_000522.3:p.Pro169= | |
| XM_017029556.1:c.506C= | XP_016885045.1:p.Pro169= | |
| NM_000531.6:c.506C= MANE Select | NP_000522.3:p.Pro169= |