Linked Data
dbSNP Id:
rs1891582845
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45480157_45480158insGATACTGT , CM000677.2:g.45480157_45480158insGATACTGT | GRCh38 |
| NC_000015.9:g.45772355_45772356insGATACTGT , CM000677.1:g.45772355_45772356insGATACTGT | GRCh37 |
| NC_000015.8:g.43559647_43559648insGATACTGT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261867.5:c.*5005_*5006insACAGTATC MANE Select | ENSP00000261867.3:n.*5005_*5006insACAGTATC | |
| ENST00000261867.4:c.*5005_*5006insACAGTATC | ENSP00000261867.3:n.*5005_*5006insACAGTATC | |
| NM_013309.5:c.*5005_*5006insACAGTATC | NP_037441.2:n.*5005_*5006insACAGTATC | |
| NM_013309.6:c.*5005_*5006insACAGTATC MANE Select | NP_037441.2:n.*5005_*5006insACAGTATC |