Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.71785007A= , CM000666.2:g.71785007A= | GRCh38 |
| NC_000004.11:g.72650724A= , CM000666.1:g.72650724A= | GRCh37 |
| NC_000004.10:g.72869588A= | NCBI36 |
| NG_012837.2:g.25514T= | |
| NG_012837.3:g.25514T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000504199.5:c.22-953T= | ENSP00000421725.1:n.22-953T= | |
| ENST00000506245.1:c.-37+913T= | ENSP00000426718.1:n.-37+913T= | |
| NM_001204306.1:c.-36-953T= | NP_001191235.1:n.-36-953T= | |
| NM_001204307.1:c.22-953T= | NP_001191236.1:n.22-953T= |