Linked Data
ClinVar Variation Id:
220912
dbSNP Id:
rs764649916
ExAC:
9:97864072 T / G
gnomAD v2:
9-97864072-T-G
gnomAD v3:
9-95101790-T-G
gnomAD v4:
9-95101790-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95101790T>G , CM000671.2:g.95101790T>G | GRCh38 |
| NC_000009.11:g.97864072T>G , CM000671.1:g.97864072T>G | GRCh37 |
| NC_000009.10:g.96903893T>G | NCBI36 |
| NG_011707.1:g.220920A>C , LRG_497:g.220920A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.410+21010T>G (AOPEP) | ||
| ENST00000696260.1:n.2409A>C (FANCC) | ||
| ENST00000289081.8:c.1594A>C (FANCC) MANE Select | ENSP00000289081.3:p.Arg532= | |
| ENST00000375305.6:c.1594A>C (FANCC) | ENSP00000364454.1:p.Arg532= | |
| ENST00000649334.1:c.1739A>C (FANCC) | ENSP00000497735.1:n.1739A>C | |
| ENST00000289081.7:c.1594A>C (FANCC) | ENSP00000289081.3:p.Arg532= | |
| ENST00000375305.5:c.1594A>C (FANCC) | ENSP00000364454.1:p.Arg532= | |
| NM_000136.2:c.1594A>C , LRG_497t1:c.1594A>C (FANCC) | NP_000127.2:p.Arg532= | |
| NM_001243743.1:c.1594A>C (FANCC) | NP_001230672.1:p.Arg532= | |
| XM_005251802.2:c.913A>C (FANCC) | XP_005251859.1:p.Arg305= | |
| XM_006717001.1:c.1429A>C (FANCC) | XP_006717064.1:p.Arg477= | |
| XM_011518365.1:c.1594A>C (FANCC) | XP_011516667.1:p.Arg532= | |
| XM_011518367.1:c.1138A>C (FANCC) | XP_011516669.1:p.Arg380= | |
| XM_011519121.1:c.2319+21010T>G (AOPEP) | XP_011517423.1:n.2319+21010T>G | |
| XM_005251802.3:c.913A>C (FANCC) | XP_005251859.1:p.Arg305= | |
| XM_006717001.3:c.1429A>C (FANCC) | XP_006717064.1:p.Arg477= | |
| XM_011518365.3:c.1594A>C (FANCC) | XP_011516667.1:p.Arg532= | |
| XM_011518367.2:c.1138A>C (FANCC) | XP_011516669.1:p.Arg380= | |
| XM_011519121.3:c.2319+21010T>G (AOPEP) | XP_011517423.1:n.2319+21010T>G | |
| XM_017014452.2:c.1138A>C (FANCC) | XP_016869941.1:p.Arg380= | |
| XM_017014453.1:c.1138A>C (FANCC) | XP_016869942.1:p.Arg380= | |
| XM_017014454.1:c.973A>C (FANCC) | XP_016869943.1:p.Arg325= | |
| XM_024447451.1:c.1594A>C (FANCC) | XP_024303219.1:p.Arg532= | |
| NM_000136.3:c.1594A>C (FANCC) MANE Select | NP_000127.2:p.Arg532= | |
| NM_001243743.2:c.1594A>C (FANCC) | NP_001230672.1:p.Arg532= |