Linked Data
dbSNP Id:
rs1761728192
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24206984_24206985del , CM000668.2:g.24206984_24206985del | GRCh38 |
| NC_000006.11:g.24207212_24207213del , CM000668.1:g.24207212_24207213del | GRCh37 |
| NC_000006.10:g.24315191_24315192del | NCBI36 |
| NG_012829.1:g.156068_156069del | |
| NG_012829.2:g.181308_181309del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.923-1883_923-1882del MANE Select | ENSP00000367715.3:n.923-1883_923-1882del | |
| ENST00000378454.7:c.923-1883_923-1882del | ENSP00000367715.3:n.923-1883_923-1882del | |
| NM_001195610.1:c.923-1883_923-1882del | NP_001182539.1:n.923-1883_923-1882del | |
| NM_016356.4:c.923-1883_923-1882del | NP_057440.2:n.923-1883_923-1882del | |
| NM_016356.5:c.923-1883_923-1882del MANE Select | NP_057440.2:n.923-1883_923-1882del | |
| NM_001195610.2:c.923-1883_923-1882del | NP_001182539.1:n.923-1883_923-1882del |