Linked Data
dbSNP Id:
rs1359171192
gnomAD v3:
22-37710724-CATGCTCCTTGGG-C
gnomAD v4:
22-37710724-CATGCTCCTTGGG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37710725_37710736del , CM000684.2:g.37710725_37710736del | GRCh38 |
| NC_000022.10:g.38106732_38106743del , CM000684.1:g.38106732_38106743del | GRCh37 |
| NC_000022.9:g.36436678_36436689del | NCBI36 |
| NG_012857.1:g.18738_18749del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.254+159_254+170del MANE Select | ENSP00000496394.1:n.254+159_254+170del | |
| ENST00000344404.10:c.254+159_254+170del | ENSP00000340312.6:n.254+159_254+170del | |
| ENST00000406386.7:c.254+159_254+170del | ENSP00000384312.3:n.254+159_254+170del | |
| ENST00000455236.4:c.1211+159_1211+170del | ENSP00000477208.1:n.1211+159_1211+170del | |
| ENST00000492485.5:n.390+159_390+170del | ||
| NM_001039141.2:c.254+159_254+170del | NP_001034230.1:n.254+159_254+170del | |
| NM_001039141.3:c.254+159_254+170del MANE Select | NP_001034230.1:n.254+159_254+170del |