Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169525867T>C , CM000663.2:g.169525867T>C | GRCh38 |
| NC_000001.10:g.169495105T>C , CM000663.1:g.169495105T>C | GRCh37 |
| NC_000001.9:g.167761729T>C | NCBI36 |
| NG_011806.1:g.65665A>G , LRG_553:g.65665A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.5716+34A>G MANE Select | ENSP00000356771.3:n.5716+34A>G | |
| ENST00000367796.3:c.5731+34A>G | ENSP00000356770.3:n.5731+34A>G | |
| ENST00000367797.7:c.5716+34A>G | ENSP00000356771.3:n.5716+34A>G | |
| NM_000130.4:c.5716+34A>G , LRG_553t1:c.5716+34A>G | NP_000121.2:n.5716+34A>G | |
| XM_017000660.2:c.5305+34A>G | XP_016856149.1:n.5305+34A>G | |
| NM_000130.5:c.5716+34A>G MANE Select | NP_000121.2:n.5716+34A>G |