Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102865911T= , CM000673.2:g.102865911T= | GRCh38 |
| NC_000011.9:g.102736642T= , CM000673.1:g.102736642T= | GRCh37 |
| NC_000011.8:g.102241852T= | NCBI36 |
| NG_032936.1:g.14124A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002426.6:c.1070A= MANE Select | NP_002417.2:p.Asn357= |
| ENST00000571244.3:c.1070A= MANE Select | ENSP00000458585.1:p.Asn357= |
| NM_002426.4:c.1070A= | NP_002417.2:p.Asn357= |
| NM_002426.5:c.1070A= | NP_002417.2:p.Asn357= |
| ENST00000571244.2:c.1070A= | ENSP00000458585.1:p.Asn357= |