Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127854293G>T , CM000671.2:g.127854293G>T | GRCh38 |
| NC_000009.11:g.130616572G>T , CM000671.1:g.130616572G>T | GRCh37 |
| NC_000009.10:g.129656393G>T | NCBI36 |
| NG_009551.1:g.5476C>A , LRG_589:g.5476C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373203.9:c.63C>A MANE Select | ENSP00000362299.4:p.Pro21= | |
| ENST00000344849.4:c.63C>A | ENSP00000341917.3:p.Pro21= | |
| ENST00000373203.8:c.63C>A | ENSP00000362299.4:p.Pro21= | |
| NM_000118.3:c.63C>A , LRG_589t1:c.63C>A | NP_000109.1:p.Pro21= | |
| NM_001114753.2:c.63C>A , LRG_589t2:c.63C>A | NP_001108225.1:p.Pro21= | |
| NM_001114753.3:c.63C>A MANE Select | NP_001108225.1:p.Pro21= |