Linked Data
dbSNP Id:
rs1567737048
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584093_41584094insCT , CM000679.2:g.41584093_41584094insCT | GRCh38 |
| NC_000017.10:g.39740345_39740346insCT , CM000679.1:g.39740345_39740346insCT | GRCh37 |
| NC_000017.9:g.36993871_36993872insCT | NCBI36 |
| NG_008624.1:g.7803_7804insGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.765+164_765+165insGA MANE Select | ENSP00000167586.6:n.765+164_765+165insGA | |
| ENST00000167586.6:c.765+164_765+165insGA | ENSP00000167586.6:n.765+164_765+165insGA | |
| ENST00000476662.1:n.215+164_215+165insGA | ||
| NM_000526.4:c.765+164_765+165insGA | NP_000517.2:n.765+164_765+165insGA | |
| NM_000526.5:c.765+164_765+165insGA MANE Select | NP_000517.3:n.765+164_765+165insGA |