Canonical Allele Identifier:
CA213119
Gene:
Linked Data
dbSNP Id:
rs1556450972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.624390_624391insGTT , CM000686.2:g.624390_624391insGTT | GRCh38 |
| NC_000024.9:g.535125_535126insGTT , CM000686.1:g.535125_535126insGTT | GRCh37 |
| NC_000024.8:g.505125_505126insGTT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711143.1:c.-645_-644insGTT | ENSP00000518641.1:n.-645_-644insGTT | |
| ENST00000711145.1:c.-645_-644insGTT | ENSP00000518642.1:n.-645_-644insGTT |