Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184060510G= , CM000665.2:g.184060510G= | GRCh38 |
| NC_000003.11:g.183778298G= , CM000665.1:g.183778298G= | GRCh37 |
| NC_000003.10:g.185260992G= | NCBI36 |
| NG_012749.1:g.12464G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_130770.3:c.*158G= MANE Select | NP_570126.2:n.*158G= |
| ENST00000318351.2:c.*158G= MANE Select | ENSP00000322617.1:n.*158G= |
| NM_130770.2:c.*158G= | NP_570126.2:n.*158G= |
| ENST00000318351.1:c.*158G= | ENSP00000322617.1:n.*158G= |