Linked Data
ClinVar Variation Id:
526329
dbSNP Id:
rs1554827151
gnomAD v3:
9-95101816-A-G
gnomAD v4:
9-95101816-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95101816A>G , CM000671.2:g.95101816A>G | GRCh38 |
| NC_000009.11:g.97864098A>G , CM000671.1:g.97864098A>G | GRCh37 |
| NC_000009.10:g.96903919A>G | NCBI36 |
| NG_011707.1:g.220894T>C , LRG_497:g.220894T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.410+21036A>G (AOPEP) | ||
| ENST00000696260.1:n.2383T>C (FANCC) | ||
| ENST00000289081.8:c.1568T>C (FANCC) MANE Select | ENSP00000289081.3:p.Ile523Thr | |
| ENST00000375305.6:c.1568T>C (FANCC) | ENSP00000364454.1:p.Ile523Thr | |
| ENST00000649334.1:c.1713T>C (FANCC) | ENSP00000497735.1:n.1713T>C | |
| ENST00000289081.7:c.1568T>C (FANCC) | ENSP00000289081.3:p.Ile523Thr | |
| ENST00000375305.5:c.1568T>C (FANCC) | ENSP00000364454.1:p.Ile523Thr | |
| NM_000136.2:c.1568T>C , LRG_497t1:c.1568T>C (FANCC) | NP_000127.2:p.Ile523Thr | |
| NM_001243743.1:c.1568T>C (FANCC) | NP_001230672.1:p.Ile523Thr | |
| XM_005251802.2:c.887T>C (FANCC) | XP_005251859.1:p.Ile296Thr | |
| XM_006717001.1:c.1403T>C (FANCC) | XP_006717064.1:p.Ile468Thr | |
| XM_011518365.1:c.1568T>C (FANCC) | XP_011516667.1:p.Ile523Thr | |
| XM_011518367.1:c.1112T>C (FANCC) | XP_011516669.1:p.Ile371Thr | |
| XM_011519121.1:c.2319+21036A>G (AOPEP) | XP_011517423.1:n.2319+21036A>G | |
| XM_005251802.3:c.887T>C (FANCC) | XP_005251859.1:p.Ile296Thr | |
| XM_006717001.3:c.1403T>C (FANCC) | XP_006717064.1:p.Ile468Thr | |
| XM_011518365.3:c.1568T>C (FANCC) | XP_011516667.1:p.Ile523Thr | |
| XM_011518367.2:c.1112T>C (FANCC) | XP_011516669.1:p.Ile371Thr | |
| XM_011519121.3:c.2319+21036A>G (AOPEP) | XP_011517423.1:n.2319+21036A>G | |
| XM_017014452.2:c.1112T>C (FANCC) | XP_016869941.1:p.Ile371Thr | |
| XM_017014453.1:c.1112T>C (FANCC) | XP_016869942.1:p.Ile371Thr | |
| XM_017014454.1:c.947T>C (FANCC) | XP_016869943.1:p.Ile316Thr | |
| XM_024447451.1:c.1568T>C (FANCC) | XP_024303219.1:p.Ile523Thr | |
| NM_000136.3:c.1568T>C (FANCC) MANE Select | NP_000127.2:p.Ile523Thr | |
| NM_001243743.2:c.1568T>C (FANCC) | NP_001230672.1:p.Ile523Thr |