Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4370676C>A , CM000674.2:g.4370676C>A | GRCh38 |
| NC_000012.11:g.4479842C>A , CM000674.1:g.4479842C>A | GRCh37 |
| NC_000012.10:g.4350103C>A | NCBI36 |
| NG_007087.1:g.14053G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020638.3:c.423G>T MANE Select | NP_065689.1:p.Ala141= |
| ENST00000237837.2:c.423G>T MANE Select | ENSP00000237837.1:p.Ala141= |
| NM_020638.2:c.423G>T | NP_065689.1:p.Ala141= |
| ENST00000237837.1:c.423G>T | ENSP00000237837.1:p.Ala141= |
| ENST00000648100.1:c.*1967+4394C>A | ENSP00000497536.1:n.*1967+4394C>A |
| ENST00000648269.1:n.1923G>T | |
| ENST00000674624.1:c.*1204+4394C>A | ENSP00000501898.1:n.*1204+4394C>A |