Linked Data
dbSNP Id:
rs2101811478
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169530687G>C , CM000663.2:g.169530687G>C | GRCh38 |
| NC_000001.10:g.169499925G>C , CM000663.1:g.169499925G>C | GRCh37 |
| NC_000001.9:g.167766549G>C | NCBI36 |
| NG_011806.1:g.60845C>G , LRG_553:g.60845C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.5208+99C>G MANE Select | ENSP00000356771.3:n.5208+99C>G | |
| ENST00000367796.3:c.5223+99C>G | ENSP00000356770.3:n.5223+99C>G | |
| ENST00000367797.7:c.5208+99C>G | ENSP00000356771.3:n.5208+99C>G | |
| NM_000130.4:c.5208+99C>G , LRG_553t1:c.5208+99C>G | NP_000121.2:n.5208+99C>G | |
| XM_017000660.2:c.4797+99C>G | XP_016856149.1:n.4797+99C>G | |
| NM_000130.5:c.5208+99C>G MANE Select | NP_000121.2:n.5208+99C>G |