Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104793G= , CM000684.2:g.32104793G= | GRCh38 |
| NC_000022.10:g.32500780G= , CM000684.1:g.32500780G= | GRCh37 |
| NC_000022.9:g.30830780G= | NCBI36 |
| NG_017045.1:g.66762G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1673G= MANE Select | ENSP00000266088.4:p.Arg558= | |
| ENST00000266088.8:c.1673G= | ENSP00000266088.4:p.Arg558= | |
| ENST00000543737.2:c.1292G= | ENSP00000444898.1:p.Arg431= | |
| NM_000343.3:c.1673G= | NP_000334.1:p.Arg558= | |
| NM_001256314.1:c.1292G= | NP_001243243.1:p.Arg431= | |
| XR_938173.1:n.591+2045C= | ||
| XR_938174.1:n.486+15062C= | ||
| NM_000343.4:c.1673G= MANE Select | NP_000334.1:p.Arg558= | |
| NM_001256314.2:c.1292G= | NP_001243243.1:p.Arg431= |