Linked Data
dbSNP Id:
rs1380428357
gnomAD v2:
6-43618293-A-G
gnomAD v3:
6-43650556-A-G
gnomAD v4:
6-43650556-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43650556A>G , CM000668.2:g.43650556A>G | GRCh38 |
| NC_000006.11:g.43618293A>G , CM000668.1:g.43618293A>G | GRCh37 |
| NC_000006.10:g.43726271A>G | NCBI36 |
| NG_023436.1:g.10527A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372163.5:c.393+16A>G (RSPH9) MANE Select | ENSP00000361236.4:n.393+16A>G | |
| ENST00000372163.4:c.393+16A>G (RSPH9) | ENSP00000361236.4:n.393+16A>G | |
| ENST00000372165.8:c.393+16A>G (RSPH9) | ENSP00000361238.4:n.393+16A>G | |
| NM_001193341.1:c.393+16A>G (RSPH9) | NP_001180270.1:n.393+16A>G | |
| NM_152732.4:c.393+16A>G (RSPH9) | NP_689945.2:n.393+16A>G | |
| XM_005248901.2:c.393+16A>G (RSPH9) | XP_005248958.1:n.393+16A>G | |
| XM_006715014.1:c.228-5006A>G (RSPH9) | XP_006715077.1:n.228-5006A>G | |
| XM_011514356.1:c.393+16A>G (RSPH9) | XP_011512658.1:n.393+16A>G | |
| XR_926099.1:n.428+16A>G (RSPH9) | ||
| XM_005248901.3:c.393+16A>G (RSPH9) | XP_005248958.1:n.393+16A>G | |
| XR_002956268.1:n.435+16A>G (RSPH9) | ||
| XR_002956269.1:n.297-5006A>G (RSPH9) | ||
| XR_926099.2:n.435+16A>G (RSPH9) | ||
| NM_152732.5:c.393+16A>G (RSPH9) MANE Select | NP_689945.2:n.393+16A>G | |
| NM_001193341.2:c.393+16A>G (RSPH9) | NP_001180270.1:n.393+16A>G | |
| NM_001318876.2:c.945+121285A>G (POLR1C) | NP_001305805.1:n.945+121285A>G |