Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129528778T>G , CM000665.2:g.129528778T>G | GRCh38 |
| NC_000003.11:g.129247621T>G , CM000665.1:g.129247621T>G | GRCh37 |
| NC_000003.10:g.130730311T>G | NCBI36 |
| NG_009115.1:g.5140T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000539.3:c.45T>G MANE Select | NP_000530.1:p.Asn15Lys |
| ENST00000296271.4:c.45T>G MANE Select | ENSP00000296271.3:p.Asn15Lys |
| ENST00000296271.3:c.45T>G | ENSP00000296271.3:p.Asn15Lys |