Linked Data
dbSNP Id:
rs869137230
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114709735dup , CM000663.2:g.114709735dup | GRCh38 |
| NC_000001.10:g.115252356dup , CM000663.1:g.115252356dup | GRCh37 |
| NC_000001.9:g.115053879dup | NCBI36 |
| NG_007572.1:g.12164dup , LRG_92:g.12164dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.291-3dup MANE Select | ENSP00000358548.4:n.291-3dup | |
| ENST00000369535.4:c.291-3dup | ENSP00000358548.4:n.291-3dup | |
| NM_002524.4:c.291-3dup | NP_002515.1:n.291-3dup | |
| NM_002524.5:c.291-3dup MANE Select | NP_002515.1:n.291-3dup |