Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189045800C= , CM000664.2:g.189045800C= | GRCh38 |
| NC_000002.11:g.189910526C= , CM000664.1:g.189910526C= | GRCh37 |
| NC_000002.10:g.189618771C= | NCBI36 |
| NG_011799.1:g.139080G= | |
| NG_011799.2:g.139080G= | |
| NG_011799.3:g.184502G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000393.5:c.3309G= MANE Select | NP_000384.2:p.Pro1103= |
| ENST00000374866.9:c.3309G= MANE Select | ENSP00000364000.3:p.Pro1103= |
| NM_000393.3:c.3309G= | NP_000384.2:p.Pro1103= |
| NM_000393.4:c.3309G= | NP_000384.2:p.Pro1103= |
| ENST00000374866.7:c.3309G= | ENSP00000364000.3:p.Pro1103= |
| ENST00000618828.1:c.2148G= | ENSP00000482184.1:p.Pro716= |
| XM_011510573.1:c.3171G= | XP_011508875.1:p.Pro1057= |
| XM_011510573.3:c.3171G= | XP_011508875.1:p.Pro1057= |