Linked Data
dbSNP Id:
rs1231182649
gnomAD v2:
9-88700090-CT-C
gnomAD v3:
9-86085175-CT-C
gnomAD v4:
9-86085175-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.86085180del , CM000671.2:g.86085180del | GRCh38 |
| NC_000009.11:g.88700095del , CM000671.1:g.88700095del | GRCh37 |
| NC_000009.10:g.87889915del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000388711.7:c.-21-5835del | ENSP00000373363.3:n.-21-5835del | |
| ENST00000388712.7:c.-21-5835del MANE Select | ENSP00000373364.3:n.-21-5835del | |
| ENST00000466178.1:c.-141-137del | ENSP00000418155.1:n.-141-137del | |
| ENST00000472919.1:n.150-5835del | ||
| NM_016548.3:c.-21-5835del | NP_057632.2:n.-21-5835del | |
| NM_177937.2:c.-21-5835del | NP_808800.1:n.-21-5835del | |
| NM_016548.4:c.-21-5835del MANE Select | NP_057632.2:n.-21-5835del | |
| NM_177937.3:c.-21-5835del | NP_808800.1:n.-21-5835del |