Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189052945C= , CM000664.2:g.189052945C= | GRCh38 |
| NC_000002.11:g.189917671C= , CM000664.1:g.189917671C= | GRCh37 |
| NC_000002.10:g.189625916C= | NCBI36 |
| NG_011799.1:g.131935G= | |
| NG_011799.2:g.131935G= | |
| NG_011799.3:g.177357G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000393.5:c.2627G= MANE Select | NP_000384.2:p.Gly876= |
| ENST00000374866.9:c.2627G= MANE Select | ENSP00000364000.3:p.Gly876= |
| NM_000393.3:c.2627G= | NP_000384.2:p.Gly876= |
| NM_000393.4:c.2627G= | NP_000384.2:p.Gly876= |
| ENST00000374866.7:c.2627G= | ENSP00000364000.3:p.Gly876= |
| ENST00000618828.1:c.1466G= | ENSP00000482184.1:p.Gly489= |
| XM_011510573.1:c.2489G= | XP_011508875.1:p.Gly830= |
| XM_011510573.3:c.2489G= | XP_011508875.1:p.Gly830= |