Linked Data
dbSNP Id:
rs1668091367
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47783028dup , CM000664.2:g.47783028dup | GRCh38 |
| NC_000002.11:g.48010167dup , CM000664.1:g.48010167dup | GRCh37 |
| NC_000002.10:g.47863671dup | NCBI36 |
| NG_007111.1:g.4882dup , LRG_219:g.4882dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652107.1:c.-37-7899dup | ENSP00000498629.1:n.-37-7899dup | |
| ENST00000606499.1:c.-37-7899dup | ENSP00000475605.1:n.-37-7899dup |