Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4379635G>C , CM000674.2:g.4379635G>C | GRCh38 |
| NC_000012.11:g.4488801G>C , CM000674.1:g.4488801G>C | GRCh37 |
| NC_000012.10:g.4359062G>C | NCBI36 |
| NG_007087.1:g.5094C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020638.3:c.-53C>G MANE Select | NP_065689.1:n.-53C>G |
| ENST00000237837.2:c.-53C>G MANE Select | ENSP00000237837.1:n.-53C>G |
| NM_020638.2:c.-53C>G | NP_065689.1:n.-53C>G |
| ENST00000237837.1:c.-53C>G | ENSP00000237837.1:n.-53C>G |
| ENST00000648100.1:c.*1967+13353G>C | ENSP00000497536.1:n.*1967+13353G>C |
| ENST00000674624.1:c.*1204+13353G>C | ENSP00000501898.1:n.*1204+13353G>C |