Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127854347G>C , CM000671.2:g.127854347G>C | GRCh38 |
| NC_000009.11:g.130616626G>C , CM000671.1:g.130616626G>C | GRCh37 |
| NC_000009.10:g.129656447G>C | NCBI36 |
| NG_009551.1:g.5422C>G , LRG_589:g.5422C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373203.9:c.9C>G MANE Select | ENSP00000362299.4:p.Arg3= | |
| ENST00000344849.4:c.9C>G | ENSP00000341917.3:p.Arg3= | |
| ENST00000373203.8:c.9C>G | ENSP00000362299.4:p.Arg3= | |
| NM_000118.3:c.9C>G , LRG_589t1:c.9C>G | NP_000109.1:p.Arg3= | |
| NM_001114753.2:c.9C>G , LRG_589t2:c.9C>G | NP_001108225.1:p.Arg3= | |
| NM_001114753.3:c.9C>G MANE Select | NP_001108225.1:p.Arg3= |