Linked Data
ClinVar Variation Id:
367597
ClinVar RCV Id:
RCV000286954
dbSNP Id:
rs150462386
gnomAD v2:
9-97863322-G-A
gnomAD v3:
9-95101040-G-A
gnomAD v4:
9-95101040-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95101040G>A , CM000671.2:g.95101040G>A | GRCh38 |
| NC_000009.11:g.97863322G>A , CM000671.1:g.97863322G>A | GRCh37 |
| NC_000009.10:g.96903143G>A | NCBI36 |
| NG_011707.1:g.221670C>T , LRG_497:g.221670C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.410+20260G>A (AOPEP) | ||
| ENST00000696260.1:n.3159C>T (FANCC) | ||
| ENST00000289081.8:c.*667C>T (FANCC) MANE Select | ENSP00000289081.3:n.*667C>T | |
| ENST00000375305.6:c.*667C>T (FANCC) | ENSP00000364454.1:n.*667C>T | |
| ENST00000289081.7:c.*667C>T (FANCC) | ENSP00000289081.3:n.*667C>T | |
| ENST00000375305.5:c.*667C>T (FANCC) | ENSP00000364454.1:n.*667C>T | |
| NM_000136.2:c.*667C>T , LRG_497t1:c.*667C>T (FANCC) | NP_000127.2:n.*667C>T | |
| NM_001243743.1:c.*667C>T (FANCC) | NP_001230672.1:n.*667C>T | |
| XM_011519121.1:c.2319+20260G>A (AOPEP) | XP_011517423.1:n.2319+20260G>A | |
| XM_005251802.3:c.*667C>T (FANCC) | XP_005251859.1:n.*667C>T | |
| XM_006717001.3:c.*667C>T (FANCC) | XP_006717064.1:n.*667C>T | |
| XM_011518365.3:c.*667C>T (FANCC) | XP_011516667.1:n.*667C>T | |
| XM_011518367.2:c.*667C>T (FANCC) | XP_011516669.1:n.*667C>T | |
| XM_011519121.3:c.2319+20260G>A (AOPEP) | XP_011517423.1:n.2319+20260G>A | |
| XM_017014452.2:c.*667C>T (FANCC) | XP_016869941.1:n.*667C>T | |
| XM_017014453.1:c.*667C>T (FANCC) | XP_016869942.1:n.*667C>T | |
| XM_017014454.1:c.*667C>T (FANCC) | XP_016869943.1:n.*667C>T | |
| XM_024447451.1:c.*667C>T (FANCC) | XP_024303219.1:n.*667C>T | |
| NM_000136.3:c.*667C>T (FANCC) MANE Select | NP_000127.2:n.*667C>T | |
| NM_001243743.2:c.*667C>T (FANCC) | NP_001230672.1:n.*667C>T |