Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763705G= , CM000674.2:g.57763705G= | GRCh38 |
| NC_000012.11:g.58157488G= , CM000674.1:g.58157488G= | GRCh37 |
| NC_000012.10:g.56443755G= | NCBI36 |
| NG_007076.1:g.8489C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000713544.1:c.1400C= | ENSP00000518840.1:p.Pro467= | |
| ENST00000713545.1:c.*324C= | ENSP00000518841.1:n.*324C= | |
| ENST00000228606.9:c.1319C= MANE Select | ENSP00000228606.4:p.Pro440= | |
| ENST00000228606.8:c.1319C= | ENSP00000228606.4:p.Pro440= | |
| ENST00000547344.5:n.1458C= | ||
| NM_000785.3:c.1319C= | NP_000776.1:p.Pro440= | |
| NM_000785.4:c.1319C= MANE Select | NP_000776.1:p.Pro440= |