Linked Data
dbSNP Id:
rs1359696642
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1394919dup , CM000667.2:g.1394919dup | GRCh38 |
| NC_000005.9:g.1395034dup , CM000667.1:g.1395034dup | GRCh37 |
| NC_000005.8:g.1448034dup | NCBI36 |
| NG_015885.1:g.55510dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1840-161dup MANE Select | ENSP00000270349.9:n.1840-161dup | |
| ENST00000270349.11:c.1840-161dup | ENSP00000270349.9:n.1840-161dup | |
| ENST00000512002.2:n.221-161dup | ||
| NM_001044.4:c.1840-161dup | NP_001035.1:n.1840-161dup | |
| NM_001044.5:c.1840-161dup MANE Select | NP_001035.1:n.1840-161dup |