Linked Data
dbSNP Id:
rs1670305650
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43887360_43887362dup , CM000664.2:g.43887360_43887362dup | GRCh38 |
| NC_000002.11:g.44114499_44114501dup , CM000664.1:g.44114499_44114501dup | GRCh37 |
| NC_000002.10:g.43968003_43968005dup | NCBI36 |
| NG_008247.1:g.113646_113648dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682612.1:c.2192_2194dup | ||
| ENST00000684454.1:n.9289_9291dup | ||
| ENST00000260665.12:c.*1240_*1242dup MANE Select | ENSP00000260665.7:n.*1240_*1242dup | |
| ENST00000260665.11:c.*1240_*1242dup | ENSP00000260665.7:n.*1240_*1242dup | |
| NM_133259.3:c.*1240_*1242dup | NP_573566.2:n.*1240_*1242dup | |
| XR_002958896.1:n.5607_5609dup | ||
| NM_133259.4:c.*1240_*1242dup MANE Select | NP_573566.2:n.*1240_*1242dup |