Linked Data
dbSNP Id:
rs1282777577
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74751965A>G , CM000677.2:g.74751965A>G | GRCh38 |
| NC_000015.9:g.75044306A>G , CM000677.1:g.75044306A>G | GRCh37 |
| NC_000015.8:g.72831359A>G | NCBI36 |
| NG_008431.1:g.34424A>G | |
| NG_008431.2:g.34424A>G | |
| NG_061543.1:g.8121A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.1042+111A>G MANE Select | ENSP00000342007.4:n.1042+111A>G | |
| ENST00000343932.4:c.1042+111A>G | ENSP00000342007.4:n.1042+111A>G | |
| NM_000761.4:c.1042+111A>G | NP_000752.2:n.1042+111A>G | |
| NM_000761.5:c.1042+111A>G MANE Select | NP_000752.2:n.1042+111A>G |