Canonical Allele Identifier:
CA2346122788
Gene:
Linked Data
dbSNP Id:
rs2085111958
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.2470983_2470984del , CM000682.2:g.2470983_2470984del | GRCh38 |
| NC_000020.10:g.2451629_2451630del , CM000682.1:g.2451629_2451630del | GRCh37 |
| NC_000020.9:g.2399629_2399630del | NCBI36 |
| NG_042057.1:g.4873_4874del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461548.1:c.305-3223_305-3222del | ENSP00000456213.1:n.305-3223_305-3222del |