Linked Data
dbSNP Id:
rs1312101931
gnomAD v2:
19-853252-TC-T
gnomAD v3:
19-853252-TC-T
gnomAD v4:
19-853252-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.853256del , CM000681.2:g.853256del | GRCh38 |
| NC_000019.9:g.853256del , CM000681.1:g.853256del | GRCh37 |
| NC_000019.8:g.804256del | NCBI36 |
| NG_009627.1:g.5966del , LRG_57:g.5966del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263621.2:c.225-6del MANE Select | ENSP00000263621.1:n.225-6del | |
| ENST00000263621.1:c.225-6del | ENSP00000263621.1:n.225-6del | |
| ENST00000590230.5:c.225-6del | ENSP00000466090.1:n.225-6del | |
| NM_001972.2:c.225-6del , LRG_57t1:c.225-6del | NP_001963.1:n.225-6del | |
| XM_011527775.1:c.225-6del | XP_011526077.1:n.225-6del | |
| XM_011527776.1:c.225-6del | XP_011526078.1:n.225-6del | |
| NM_001972.3:c.225-6del | NP_001963.1:n.225-6del | |
| NM_001972.4:c.225-6del MANE Select | NP_001963.1:n.225-6del |