Linked Data
dbSNP Id:
rs1225884693
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91107219_91107220dup , CM000674.2:g.91107219_91107220dup | GRCh38 |
| NC_000012.11:g.91500996_91500997dup , CM000674.1:g.91500996_91500997dup | GRCh37 |
| NC_000012.10:g.90025127_90025128dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.5:c.862+903_862+904dup MANE Select | ENSP00000266718.4:n.862+903_862+904dup | |
| ENST00000266718.4:c.862+903_862+904dup | ENSP00000266718.4:n.862+903_862+904dup | |
| ENST00000546642.1:n.612+903_612+904dup | ||
| ENST00000548071.1:n.255+903_255+904dup | ||
| NM_002345.3:c.862+903_862+904dup | NP_002336.1:n.862+903_862+904dup | |
| NM_002345.4:c.862+903_862+904dup MANE Select | NP_002336.1:n.862+903_862+904dup |