Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151261427A= , CM000668.2:g.151261427A= | GRCh38 |
| NC_000006.11:g.151582562A= , CM000668.1:g.151582562A= | GRCh37 |
| NC_000006.10:g.151624255A= | NCBI36 |
| NG_029875.1:g.26429A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005100.4:c.162+20703A= MANE Select | NP_005091.2:n.162+20703A= |
| ENST00000402676.7:c.162+20703A= MANE Select | ENSP00000384537.2:n.162+20703A= |
| NM_005100.3:c.162+20703A= | NP_005091.2:n.162+20703A= |
| ENST00000253332.5:c.162+20703A= | ENSP00000253332.1:n.162+20703A= |
| ENST00000402676.6:c.162+20703A= | ENSP00000384537.2:n.162+20703A= |
| XM_005267233.1:c.162+20703A= | XP_005267290.1:n.162+20703A= |
| XM_017011517.2:c.162+20703A= | XP_016867006.1:n.162+20703A= |