Linked Data
dbSNP Id:
rs748097778
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100883086G>T , CM000676.2:g.100883086G>T | GRCh38 |
| NC_000014.8:g.101349423G>T , CM000676.1:g.101349423G>T | GRCh37 |
| NC_000014.7:g.100419176G>T | NCBI36 |
| NG_045001.1:g.6762C>A | |
| NG_045000.5:g.51818G>T | |
| NG_045000.6:g.51818G>T | |
| NG_045001.2:g.25637C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1703C>A MANE Select | ENSP00000497482.1:p.Pro568Gln | |
| ENST00000534062.1:c.1703C>A | ENSP00000435342.1:p.Pro568Gln | |
| NM_001134888.2:c.1703C>A | NP_001128360.1:p.Pro568Gln | |
| NM_001134888.3:c.1703C>A MANE Select | NP_001128360.1:p.Pro568Gln |