Linked Data
dbSNP Id:
rs2092603229
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927978dup , CM000663.2:g.149927978dup | GRCh38 |
| NC_000001.10:g.149899870dup , CM000663.1:g.149899870dup | GRCh37 |
| NC_000001.9:g.148166494dup | NCBI36 |
| NG_032777.1:g.5275dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-219dup | ENSP00000271628.8:n.-219dup | |
| NM_005850.4:c.-219dup | NP_005841.1:n.-219dup |