Canonical Allele Identifier:
CA632429685
Gene:
Linked Data
dbSNP Id:
rs1259964799
gnomAD v2:
19-20328960-CA-C
gnomAD v3:
19-20218151-CA-C
gnomAD v4:
19-20218151-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20218156del , CM000681.2:g.20218156del | GRCh38 |
| NC_000019.9:g.20328965del , CM000681.1:g.20328965del | GRCh37 |
| NC_000019.8:g.20189965del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-836del | ||
| XR_936389.1:n.502-836del | ||
| XR_936390.1:n.511-836del | ||
| XR_936391.1:n.514-836del | ||
| XR_936392.1:n.514-836del | ||
| XR_936394.1:n.41-578del | ||
| XR_001754063.2:n.1506-836del | ||
| XR_001754064.2:n.138-836del | ||
| XR_001754066.1:n.3912-836del | ||
| XR_001754067.1:n.3912-836del | ||
| XR_001754068.1:n.3912-836del | ||
| XR_936394.2:n.41-578del | ||
| XR_936406.2:n.1411-836del |