Linked Data
dbSNP Id:
rs987994658
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150992522C>G , CM000669.2:g.150992522C>G | GRCh38 |
| NC_000007.13:g.150689610C>G , CM000669.1:g.150689610C>G | GRCh37 |
| NC_000007.12:g.150320543C>G | NCBI36 |
| NG_011992.1:g.6464C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297494.8:c.-52+1222C>G MANE Select | ENSP00000297494.3:n.-52+1222C>G | |
| ENST00000297494.7:c.-52+1222C>G | ENSP00000297494.3:n.-52+1222C>G | |
| ENST00000461406.5:c.-149+1222C>G | ENSP00000417143.1:n.-149+1222C>G | |
| NM_000603.4:c.-52+1222C>G | NP_000594.2:n.-52+1222C>G | |
| NM_000603.5:c.-52+1222C>G MANE Select | NP_000594.2:n.-52+1222C>G |