Linked Data
dbSNP Id:
rs2089443650
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20778616G>A , CM000686.2:g.20778616G>A | GRCh38 |
| NC_000024.9:g.22940502G>A , CM000686.1:g.22940502G>A | GRCh37 |
| NC_000024.8:g.21349890G>A | NCBI36 |
| NG_032924.1:g.27549G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000629237.2:c.533-893G>A MANE Select | ENSP00000486252.1:n.533-893G>A | |
| ENST00000629237.1:c.533-893G>A | ENSP00000486252.1:n.533-893G>A | |
| NM_001039567.2:c.533-893G>A | NP_001034656.1:n.533-893G>A | |
| XM_011531423.1:c.482-893G>A | XP_011529725.1:n.482-893G>A | |
| NM_001039567.3:c.533-893G>A MANE Select | NP_001034656.1:n.533-893G>A |