Linked Data
dbSNP Id:
rs1735210187
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268548_77268549insTCT , CM000680.2:g.77268548_77268549insTCT | GRCh38 |
| NC_000018.9:g.74980504_74980505insTCT , CM000680.1:g.74980504_74980505insTCT | GRCh37 |
| NC_000018.8:g.73109492_73109493insTCT | NCBI36 |
| NG_009223.1:g.23497_23498insTCT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-37_733-36insTCT MANE Select | ENSP00000299727.3:n.733-37_733-36insTCT | |
| ENST00000299727.4:c.733-37_733-36insTCT | ENSP00000299727.3:n.733-37_733-36insTCT | |
| NM_001480.3:c.733-37_733-36insTCT | NP_001471.2:n.733-37_733-36insTCT | |
| NM_001480.4:c.733-37_733-36insTCT MANE Select | NP_001471.2:n.733-37_733-36insTCT |