Linked Data
dbSNP Id:
rs1960072598
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23211119C>G , CM000678.2:g.23211119C>G | GRCh38 |
| NC_000016.9:g.23222440C>G , CM000678.1:g.23222440C>G | GRCh37 |
| NC_000016.8:g.23129941C>G | NCBI36 |
| NG_011909.1:g.33401C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300061.3:c.1177-915C>G MANE Select | ENSP00000300061.2:n.1177-915C>G | |
| ENST00000300061.2:c.1177-915C>G | ENSP00000300061.2:n.1177-915C>G | |
| NM_001039.3:c.1177-915C>G | NP_001030.2:n.1177-915C>G | |
| NM_001039.4:c.1177-915C>G MANE Select | NP_001030.2:n.1177-915C>G |