Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4372649C>G , CM000674.2:g.4372649C>G | GRCh38 |
| NC_000012.11:g.4481815C>G , CM000674.1:g.4481815C>G | GRCh37 |
| NC_000012.10:g.4352076C>G | NCBI36 |
| NG_007087.1:g.12080G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237837.2:c.260G>C MANE Select | ENSP00000237837.1:p.Gly87Ala | |
| ENST00000648100.1:c.*1967+6367C>G | ENSP00000497536.1:n.*1967+6367C>G | |
| ENST00000648269.1:n.1760G>C | ||
| ENST00000674624.1:c.*1204+6367C>G | ENSP00000501898.1:n.*1204+6367C>G | |
| ENST00000237837.1:c.260G>C | ENSP00000237837.1:p.Gly87Ala | |
| NM_020638.2:c.260G>C | NP_065689.1:p.Gly87Ala | |
| NM_020638.3:c.260G>C MANE Select | NP_065689.1:p.Gly87Ala |