Canonical Allele Identifier:
CA632429684
Gene:
Linked Data
dbSNP Id:
rs1555721024
gnomAD v2:
19-20328951-TTC-T
gnomAD v3:
19-20218142-TTC-T
gnomAD v4:
19-20218142-TTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20218144_20218145del , CM000681.2:g.20218144_20218145del | GRCh38 |
| NC_000019.9:g.20328953_20328954del , CM000681.1:g.20328953_20328954del | GRCh37 |
| NC_000019.8:g.20189953_20189954del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-828_619-827del | ||
| XR_936389.1:n.502-828_502-827del | ||
| XR_936390.1:n.511-828_511-827del | ||
| XR_936391.1:n.514-828_514-827del | ||
| XR_936392.1:n.514-828_514-827del | ||
| XR_936394.1:n.41-590_41-589del | ||
| XR_001754063.2:n.1506-828_1506-827del | ||
| XR_001754064.2:n.138-828_138-827del | ||
| XR_001754066.1:n.3912-828_3912-827del | ||
| XR_001754067.1:n.3912-828_3912-827del | ||
| XR_001754068.1:n.3912-828_3912-827del | ||
| XR_936394.2:n.41-590_41-589del | ||
| XR_936406.2:n.1411-828_1411-827del |