Linked Data
dbSNP Id:
rs545056897
gnomAD v2:
8-118089547-C-T
gnomAD v3:
8-117077308-C-T
gnomAD v4:
8-117077308-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117077308C>T , CM000670.2:g.117077308C>T | GRCh38 |
| NC_000008.10:g.118089547C>T , CM000670.1:g.118089547C>T | GRCh37 |
| NC_000008.9:g.118158728C>T | NCBI36 |
| NG_016991.1:g.132036C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000427715.2:c.-226+38050C>T | ENSP00000407505.2:n.-226+38050C>T | |
| ENST00000521035.5:n.295-57924C>T | ||
| ENST00000521243.5:c.-106-69511C>T | ENSP00000428545.1:n.-106-69511C>T | |
| ENST00000524274.5:c.-106-69511C>T | ENSP00000427760.1:n.-106-69511C>T | |
| NM_001172811.1:c.-106-69511C>T | NP_001166282.1:n.-106-69511C>T | |
| NM_001172813.1:c.-273-57924C>T | NP_001166284.1:n.-273-57924C>T | |
| NM_001172815.1:c.-226+38050C>T | NP_001166286.1:n.-226+38050C>T | |
| XM_011516881.1:c.-96-57924C>T | XP_011515183.1:n.-96-57924C>T | |
| NM_001172815.2:c.-226+38050C>T | NP_001166286.1:n.-226+38050C>T | |
| XM_024447083.1:c.-106-69511C>T | XP_024302851.1:n.-106-69511C>T | |
| NM_001172811.2:c.-106-69511C>T | NP_001166282.1:n.-106-69511C>T | |
| NM_001172813.2:c.-273-57924C>T | NP_001166284.1:n.-273-57924C>T | |
| NM_001172815.3:c.-226+38050C>T | NP_001166286.1:n.-226+38050C>T |