Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.46310465A= , CM000664.2:g.46310465A= | GRCh38 |
| NC_000002.11:g.46537604A= , CM000664.1:g.46537604A= | GRCh37 |
| NC_000002.10:g.46391108A= | NCBI36 |
| NG_016000.1:g.18064A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263734.5:c.26+12528A= MANE Select | ENSP00000263734.3:n.26+12528A= | |
| ENST00000263734.4:c.26+12528A= | ENSP00000263734.3:n.26+12528A= | |
| ENST00000449347.5:c.26+12528A= | ENSP00000406137.1:n.26+12528A= | |
| ENST00000460015.1:n.432+16367A= | ||
| ENST00000467888.5:n.174+12528A= | ||
| NM_001430.4:c.26+12528A= | NP_001421.2:n.26+12528A= | |
| XR_940055.1:n.2501+3628T= | ||
| NM_001430.5:c.26+12528A= MANE Select | NP_001421.2:n.26+12528A= |