Linked Data
ClinVar Variation Id:
1990473
ClinVar RCV Id:
RCV002771354
dbSNP Id:
rs145904853
ExAC:
12:45781927 T / C
gnomAD v2:
12-45781927-T-C
gnomAD v3:
12-45388144-T-C
gnomAD v4:
12-45388144-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.45388144T>C , CM000674.2:g.45388144T>C | GRCh38 |
| NC_000012.11:g.45781927T>C , CM000674.1:g.45781927T>C | GRCh37 |
| NC_000012.10:g.44068194T>C | NCBI36 |
| NG_028220.1:g.177158T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320560.13:c.1166-17T>C MANE Select | ENSP00000320087.8:n.1166-17T>C | |
| ENST00000679426.1:c.1133-17T>C | ENSP00000506600.1:n.1133-17T>C | |
| ENST00000679761.1:c.1166-17T>C | ENSP00000505361.1:n.1166-17T>C | |
| ENST00000680201.1:c.1166-17T>C | ENSP00000506222.1:n.1166-17T>C | |
| ENST00000680371.1:c.1166-17T>C | ENSP00000506392.1:n.1166-17T>C | |
| ENST00000680498.1:c.749-17T>C | ENSP00000506613.1:n.749-17T>C | |
| ENST00000681156.1:c.1166-17T>C | ENSP00000506069.1:n.1166-17T>C | |
| ENST00000681817.1:c.749-17T>C | ENSP00000506683.1:n.749-17T>C | |
| ENST00000320560.12:c.1166-17T>C | ENSP00000320087.8:n.1166-17T>C | |
| ENST00000423947.7:c.1229-17T>C | ENSP00000409126.3:n.1229-17T>C | |
| ENST00000425752.6:c.1166-17T>C | ENSP00000391417.2:n.1166-17T>C | |
| ENST00000426898.2:n.1582-17T>C | ||
| ENST00000441606.2:c.1112-17T>C | ENSP00000413137.2:n.1112-17T>C | |
| NM_001025356.2:c.1166-17T>C | NP_001020527.2:n.1166-17T>C | |
| NM_001142678.1:c.1112-17T>C | NP_001136150.1:n.1112-17T>C | |
| NM_001142679.1:c.1166-17T>C | NP_001136151.1:n.1166-17T>C | |
| NM_001204803.1:c.1229-17T>C | NP_001191732.1:n.1229-17T>C | |
| XM_005268706.3:c.1133-17T>C | XP_005268763.1:n.1133-17T>C | |
| XM_005268707.2:c.1067-17T>C | XP_005268764.1:n.1067-17T>C | |
| XM_011538024.1:c.1229-17T>C | XP_011536326.1:n.1229-17T>C | |
| XR_944888.1:n.1406-9613A>G | ||
| XM_005268706.5:c.1133-17T>C | XP_005268763.1:n.1133-17T>C | |
| XM_005268707.4:c.1067-17T>C | XP_005268764.1:n.1067-17T>C | |
| NM_001025356.3:c.1166-17T>C MANE Select | NP_001020527.2:n.1166-17T>C | |
| NM_001142678.2:c.1112-17T>C | NP_001136150.1:n.1112-17T>C | |
| NM_001142679.2:c.1166-17T>C | NP_001136151.1:n.1166-17T>C | |
| NM_001204803.2:c.1229-17T>C | NP_001191732.1:n.1229-17T>C |