Linked Data
dbSNP Id:
rs1891582944
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45480161dup , CM000677.2:g.45480161dup | GRCh38 |
| NC_000015.9:g.45772359dup , CM000677.1:g.45772359dup | GRCh37 |
| NC_000015.8:g.43559651dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261867.5:c.*5002dup MANE Select | ENSP00000261867.3:n.*5002dup | |
| ENST00000261867.4:c.*5002dup | ENSP00000261867.3:n.*5002dup | |
| NM_013309.5:c.*5002dup | NP_037441.2:n.*5002dup | |
| NM_013309.6:c.*5002dup MANE Select | NP_037441.2:n.*5002dup |