Linked Data
dbSNP Id:
rs2049664857
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78118273_78118274del , CM000685.2:g.78118273_78118274del | GRCh38 |
| NC_000023.10:g.77373770_77373771del , CM000685.1:g.77373770_77373771del | GRCh37 |
| NC_000023.9:g.77260426_77260427del | NCBI36 |
| NG_008862.1:g.19105_19106del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.641+103_641+104del MANE Select | ENSP00000362413.4:n.641+103_641+104del | |
| ENST00000644362.1:c.557+103_557+104del | ENSP00000496140.1:n.557+103_557+104del | |
| ENST00000373316.4:c.641+103_641+104del | ENSP00000362413.4:n.641+103_641+104del | |
| ENST00000491291.1:n.633+103_633+104del | ||
| NM_000291.3:c.641+103_641+104del | NP_000282.1:n.641+103_641+104del | |
| NM_000291.4:c.641+103_641+104del MANE Select | NP_000282.1:n.641+103_641+104del |