Canonical Allele Identifier:
CA2002397796
Gene:
Linked Data
dbSNP Id:
rs1864211443
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116072631_116072639del , CM000673.2:g.116072631_116072639del | GRCh38 |
| NC_000011.9:g.115943349_115943357del , CM000673.1:g.115943349_115943357del | GRCh37 |
| NC_000011.8:g.115448559_115448567del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948055.1:n.192+375_192+383del | ||
| XR_948056.1:n.311-5434_311-5426del | ||
| XR_948057.1:n.97+470_97+478del | ||
| XR_001748401.1:n.192+375_192+383del | ||
| XR_948055.2:n.192+375_192+383del | ||
| XR_948056.2:n.314-5434_314-5426del | ||
| XR_948057.2:n.97+470_97+478del |