Linked Data
ClinVar Variation Id:
127544
ClinVar RCV Id:
RCV000120979
RCV000200372
RCV000570280
RCV000709090
RCV000988214
RCV001195037
RCV001356599
RCV003945045
dbSNP Id:
rs140781259
ExAC:
9:97912259 G / C
gnomAD v2:
9-97912259-G-C
gnomAD v3:
9-95149977-G-C
gnomAD v4:
9-95149977-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95149977G>C , CM000671.2:g.95149977G>C | GRCh38 |
| NC_000009.11:g.97912259G>C , CM000671.1:g.97912259G>C | GRCh37 |
| NC_000009.10:g.96952080G>C | NCBI36 |
| NG_011707.1:g.172733C>G , LRG_497:g.172733C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.3177G>C (AOPEP) | ||
| ENST00000696261.1:n.1023C>G (FANCC) | ||
| ENST00000289081.8:c.632C>G (FANCC) MANE Select | ENSP00000289081.3:p.Pro211Arg | |
| ENST00000375305.6:c.632C>G (FANCC) | ENSP00000364454.1:p.Pro211Arg | |
| ENST00000490972.7:c.632C>G (FANCC) | ENSP00000479931.1:p.Pro211Arg | |
| ENST00000649334.1:c.777C>G (FANCC) | ENSP00000497735.1:n.777C>G | |
| ENST00000649701.1:n.347C>G (FANCC) | ||
| ENST00000289081.7:c.632C>G (FANCC) | ENSP00000289081.3:p.Pro211Arg | |
| ENST00000375305.5:c.632C>G (FANCC) | ENSP00000364454.1:p.Pro211Arg | |
| ENST00000490972.6:c.632C>G (FANCC) | ENSP00000479931.1:p.Pro211Arg | |
| ENST00000493098.1:n.57C>G (FANCC) | ||
| NM_000136.2:c.632C>G , LRG_497t1:c.632C>G (FANCC) | NP_000127.2:p.Pro211Arg | |
| NM_001243743.1:c.632C>G (FANCC) | NP_001230672.1:p.Pro211Arg | |
| NM_001243744.1:c.632C>G (FANCC) | NP_001230673.1:p.Pro211Arg | |
| XM_006717001.1:c.522-14475C>G (FANCC) | XP_006717064.1:n.522-14475C>G | |
| XM_006717002.2:c.632C>G (FANCC) | XP_006717065.1:p.Pro211Arg | |
| XM_006717004.2:c.632C>G (FANCC) | XP_006717067.1:p.Pro211Arg | |
| XM_011518365.1:c.632C>G (FANCC) | XP_011516667.1:p.Pro211Arg | |
| XM_011518366.1:c.632C>G (FANCC) | XP_011516668.1:p.Pro211Arg | |
| XM_011518367.1:c.176C>G (FANCC) | XP_011516669.1:p.Pro59Arg | |
| XM_006717001.3:c.522-14475C>G (FANCC) | XP_006717064.1:n.522-14475C>G | |
| XM_006717002.4:c.632C>G (FANCC) | XP_006717065.1:p.Pro211Arg | |
| XM_006717004.4:c.632C>G (FANCC) | XP_006717067.1:p.Pro211Arg | |
| XM_011518365.3:c.632C>G (FANCC) | XP_011516667.1:p.Pro211Arg | |
| XM_011518366.3:c.632C>G (FANCC) | XP_011516668.1:p.Pro211Arg | |
| XM_011518367.2:c.176C>G (FANCC) | XP_011516669.1:p.Pro59Arg | |
| XM_017014452.2:c.176C>G (FANCC) | XP_016869941.1:p.Pro59Arg | |
| XM_017014453.1:c.176C>G (FANCC) | XP_016869942.1:p.Pro59Arg | |
| XM_017014454.1:c.66-14475C>G (FANCC) | XP_016869943.1:n.66-14475C>G | |
| XM_024447451.1:c.632C>G (FANCC) | XP_024303219.1:p.Pro211Arg | |
| NM_000136.3:c.632C>G (FANCC) MANE Select | NP_000127.2:p.Pro211Arg | |
| NM_001243743.2:c.632C>G (FANCC) | NP_001230672.1:p.Pro211Arg | |
| NM_001243744.2:c.632C>G (FANCC) | NP_001230673.1:p.Pro211Arg |