Linked Data
ClinVar Variation Id:
189053
dbSNP Id:
rs774209201
ExAC:
9:97888864 C / G
gnomAD v2:
9-97888864-C-G
gnomAD v3:
9-95126582-C-G
gnomAD v4:
9-95126582-C-G
PubMed:
PMID:17924555
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95126582C>G , CM000671.2:g.95126582C>G | GRCh38 |
| NC_000009.11:g.97888864C>G , CM000671.1:g.97888864C>G | GRCh37 |
| NC_000009.10:g.96928685C>G | NCBI36 |
| NG_011707.1:g.196128G>C , LRG_497:g.196128G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.411-20629C>G (AOPEP) | ||
| ENST00000289081.8:c.844-1G>C (FANCC) MANE Select | ENSP00000289081.3:n.844-1G>C | |
| ENST00000375305.6:c.844-1G>C (FANCC) | ENSP00000364454.1:n.844-1G>C | |
| ENST00000490972.7:c.844-1G>C (FANCC) | ENSP00000479931.1:n.844-1G>C | |
| ENST00000649334.1:c.989-1G>C (FANCC) | ENSP00000497735.1:n.989-1G>C | |
| ENST00000289081.7:c.844-1G>C (FANCC) | ENSP00000289081.3:n.844-1G>C | |
| ENST00000375305.5:c.844-1G>C (FANCC) | ENSP00000364454.1:n.844-1G>C | |
| ENST00000464627.5:n.171-1G>C (FANCC) | ||
| ENST00000464653.1:n.839G>C (FANCC) | ||
| ENST00000477942.5:n.199-1G>C (FANCC) | ||
| ENST00000480712.5:n.29-1G>C (FANCC) | ||
| ENST00000490972.6:c.844-1G>C (FANCC) | ENSP00000479931.1:n.844-1G>C | |
| NM_000136.2:c.844-1G>C , LRG_497t1:c.844-1G>C (FANCC) | NP_000127.2:n.844-1G>C | |
| NM_001243743.1:c.844-1G>C (FANCC) | NP_001230672.1:n.844-1G>C | |
| NM_001243744.1:c.844-1G>C (FANCC) | NP_001230673.1:n.844-1G>C | |
| XM_005251802.2:c.163-1G>C (FANCC) | XP_005251859.1:n.163-1G>C | |
| XM_006717001.1:c.679-1G>C (FANCC) | XP_006717064.1:n.679-1G>C | |
| XM_006717002.2:c.844-1G>C (FANCC) | XP_006717065.1:n.844-1G>C | |
| XM_006717004.2:c.844-1G>C (FANCC) | XP_006717067.1:n.844-1G>C | |
| XM_011518365.1:c.844-1G>C (FANCC) | XP_011516667.1:n.844-1G>C | |
| XM_011518366.1:c.844-1G>C (FANCC) | XP_011516668.1:n.844-1G>C | |
| XM_011518367.1:c.388-1G>C (FANCC) | XP_011516669.1:n.388-1G>C | |
| XM_011519121.1:c.2320-20629C>G (AOPEP) | XP_011517423.1:n.2320-20629C>G | |
| XM_005251802.3:c.163-1G>C (FANCC) | XP_005251859.1:n.163-1G>C | |
| XM_006717001.3:c.679-1G>C (FANCC) | XP_006717064.1:n.679-1G>C | |
| XM_006717002.4:c.844-1G>C (FANCC) | XP_006717065.1:n.844-1G>C | |
| XM_006717004.4:c.844-1G>C (FANCC) | XP_006717067.1:n.844-1G>C | |
| XM_011518365.3:c.844-1G>C (FANCC) | XP_011516667.1:n.844-1G>C | |
| XM_011518366.3:c.844-1G>C (FANCC) | XP_011516668.1:n.844-1G>C | |
| XM_011518367.2:c.388-1G>C (FANCC) | XP_011516669.1:n.388-1G>C | |
| XM_011519121.3:c.2320-20629C>G (AOPEP) | XP_011517423.1:n.2320-20629C>G | |
| XM_017014452.2:c.388-1G>C (FANCC) | XP_016869941.1:n.388-1G>C | |
| XM_017014453.1:c.388-1G>C (FANCC) | XP_016869942.1:n.388-1G>C | |
| XM_017014454.1:c.223-1G>C (FANCC) | XP_016869943.1:n.223-1G>C | |
| XM_024447451.1:c.844-1G>C (FANCC) | XP_024303219.1:n.844-1G>C | |
| NM_000136.3:c.844-1G>C (FANCC) MANE Select | NP_000127.2:n.844-1G>C | |
| NM_001243743.2:c.844-1G>C (FANCC) | NP_001230672.1:n.844-1G>C | |
| NM_001243744.2:c.844-1G>C (FANCC) | NP_001230673.1:n.844-1G>C |