Linked Data
dbSNP Id:
rs566834189
gnomAD v2:
13-33610073-TA-T
gnomAD v3:
13-33035936-TA-T
gnomAD v4:
13-33035936-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33035937del , CM000675.2:g.33035937del | GRCh38 |
| NC_000013.10:g.33610074del , CM000675.1:g.33610074del | GRCh37 |
| NC_000013.9:g.32508074del | NCBI36 |
| NG_011485.1:g.24504del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380099.4:c.820-17830del MANE Select | ENSP00000369442.3:n.820-17830del | |
| ENST00000380099.3:c.820-17830del | ENSP00000369442.3:n.820-17830del | |
| ENST00000487852.1:n.828-17830del | ||
| NM_004795.3:c.820-17830del | NP_004786.2:n.820-17830del | |
| XM_006719895.1:c.-102-17830del | XP_006719958.1:n.-102-17830del | |
| XM_006719895.2:c.-102-17830del | XP_006719958.1:n.-102-17830del | |
| NM_004795.4:c.820-17830del MANE Select | NP_004786.2:n.820-17830del |