Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110911077C>T , CM000674.2:g.110911077C>T | GRCh38 |
| NC_000012.11:g.111348881C>T , CM000674.1:g.111348881C>T | GRCh37 |
| NC_000012.10:g.109833264C>T | NCBI36 |
| NG_007554.1:g.14501G>A , LRG_393:g.14501G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228841.15:c.501G>A MANE Select | ENSP00000228841.8:p.Ter167= | |
| ENST00000663220.1:c.444G>A | ENSP00000499568.1:p.Ter148= | |
| ENST00000228841.12:c.501G>A | ENSP00000228841.7:p.Ter167= | |
| ENST00000548438.1:c.459G>A | ENSP00000447154.1:p.Ter153= | |
| NM_000432.3:c.501G>A , LRG_393t1:c.501G>A | NP_000423.2:p.Ter167= | |
| NM_000432.4:c.501G>A MANE Select | NP_000423.2:p.Ter167= |