Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127854208A>G , CM000671.2:g.127854208A>G | GRCh38 |
| NC_000009.11:g.130616487A>G , CM000671.1:g.130616487A>G | GRCh37 |
| NC_000009.10:g.129656308A>G | NCBI36 |
| NG_009551.1:g.5561T>C , LRG_589:g.5561T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373203.9:c.67+81T>C MANE Select | ENSP00000362299.4:n.67+81T>C | |
| ENST00000344849.4:c.67+81T>C | ENSP00000341917.3:n.67+81T>C | |
| ENST00000373203.8:c.67+81T>C | ENSP00000362299.4:n.67+81T>C | |
| NM_000118.3:c.67+81T>C , LRG_589t1:c.67+81T>C | NP_000109.1:n.67+81T>C | |
| NM_001114753.2:c.67+81T>C , LRG_589t2:c.67+81T>C | NP_001108225.1:n.67+81T>C | |
| NM_001114753.3:c.67+81T>C MANE Select | NP_001108225.1:n.67+81T>C |