Canonical Allele Identifier:
CA914464098
Gene:
Linked Data
dbSNP Id:
rs1558785894
gnomAD v2:
2-123641680-GT-G
gnomAD v3:
2-122884104-GT-G
gnomAD v4:
2-122884104-GT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122884107del , CM000664.2:g.122884107del | GRCh38 |
| NC_000002.11:g.123641683del , CM000664.1:g.123641683del | GRCh37 |
| NC_000002.10:g.123358153del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923292.1:n.1125-835del | ||
| XR_001739692.1:n.1451-835del | ||
| XR_923292.2:n.1358-835del |