Canonical Allele Identifier:
CA916587234
Gene:
Linked Data
dbSNP Id:
rs1558824387
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88015997dup , CM000664.2:g.88015997dup | GRCh38 |
| NC_000002.11:g.88315516dup , CM000664.1:g.88315516dup | GRCh37 |
| NC_000002.10:g.88096631dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.342dup | ||
| XR_940336.3:n.342dup |