Linked Data
dbSNP Id:
rs2057244286
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665083dup , CM000679.2:g.39665083dup | GRCh38 |
| NC_000017.10:g.37821336dup , CM000679.1:g.37821336dup | GRCh37 |
| NC_000017.9:g.35074862dup | NCBI36 |
| NG_008892.1:g.4738dup , LRG_210:g.4738dup | |
| NG_042278.1:g.2103dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.2:c.-277dup | ENSP00000312624.2:n.-277dup |