Linked Data
dbSNP Id:
rs1427319633
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780609A>G , CM000672.2:g.94780609A>G | GRCh38 |
| NC_000010.10:g.96540366A>G , CM000672.1:g.96540366A>G | GRCh37 |
| NC_000010.9:g.96530356A>G | NCBI36 |
| NG_008384.2:g.22904A>G | |
| NG_008384.3:g.22929A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.592A>G MANE Select | ENSP00000360372.3:p.Met198Val | |
| ENST00000645461.1:n.1645A>G | ||
| ENST00000371321.7:c.592A>G | ENSP00000360372.3:p.Met198Val | |
| ENST00000464755.1:c.1355A>G | ENSP00000483243.1:n.1355A>G | |
| NM_000769.2:c.592A>G | NP_000760.1:p.Met198Val | |
| NM_000769.4:c.592A>G MANE Select | NP_000760.1:p.Met198Val |