Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110820191A>G , CM000672.2:g.110820191A>G | GRCh38 |
| NC_000010.10:g.112579949A>G , CM000672.1:g.112579949A>G | GRCh37 |
| NC_000010.9:g.112569939A>G | NCBI36 |
| NG_021177.1:g.180795A>G , LRG_382:g.180795A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.2655+15A>G MANE Select | ENSP00000358532.3:n.2655+15A>G | |
| ENST00000369519.3:c.2655+15A>G | ENSP00000358532.3:n.2655+15A>G | |
| NM_001134363.2:c.2655+15A>G | NP_001127835.2:n.2655+15A>G | |
| XM_011539697.1:c.2271+15A>G | XP_011537999.1:n.2271+15A>G | |
| XM_017016103.2:c.2490+15A>G | XP_016871592.1:n.2490+15A>G | |
| XM_017016104.2:c.2271+15A>G | XP_016871593.1:n.2271+15A>G | |
| NM_001134363.3:c.2655+15A>G MANE Select | NP_001127835.2:n.2655+15A>G |