Linked Data
ClinVar Variation Id:
1544283
ClinVar RCV Id:
RCV002182296
dbSNP Id:
rs2135428712
gnomAD v4:
9-95150069-C-T
MyVariant Identifiers:
chr9:g.97912351C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95150069C>T , CM000671.2:g.95150069C>T | GRCh38 |
| NC_000009.11:g.97912351C>T , CM000671.1:g.97912351C>T | GRCh37 |
| NC_000009.10:g.96952172C>T | NCBI36 |
| NG_011707.1:g.172641G>A , LRG_497:g.172641G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710812.1:n.3269C>T (AOPEP) | ||
| ENST00000696261.1:n.931G>A (FANCC) | ||
| ENST00000289081.8:c.540G>A (FANCC) MANE Select | ENSP00000289081.3:p.Val180= | |
| ENST00000375305.6:c.540G>A (FANCC) | ENSP00000364454.1:p.Val180= | |
| ENST00000490972.7:c.540G>A (FANCC) | ENSP00000479931.1:p.Val180= | |
| ENST00000636777.1:n.598G>A (FANCC) | ||
| ENST00000649334.1:c.685G>A (FANCC) | ENSP00000497735.1:n.685G>A | |
| ENST00000649701.1:n.255G>A (FANCC) | ||
| ENST00000289081.7:c.540G>A (FANCC) | ENSP00000289081.3:p.Val180= | |
| ENST00000375305.5:c.540G>A (FANCC) | ENSP00000364454.1:p.Val180= | |
| ENST00000490972.6:c.540G>A (FANCC) | ENSP00000479931.1:p.Val180= | |
| NM_000136.2:c.540G>A , LRG_497t1:c.540G>A (FANCC) | NP_000127.2:p.Val180= | |
| NM_001243743.1:c.540G>A (FANCC) | NP_001230672.1:p.Val180= | |
| NM_001243744.1:c.540G>A (FANCC) | NP_001230673.1:p.Val180= | |
| XM_006717001.1:c.522-14567G>A (FANCC) | XP_006717064.1:n.522-14567G>A | |
| XM_006717002.2:c.540G>A (FANCC) | XP_006717065.1:p.Val180= | |
| XM_006717004.2:c.540G>A (FANCC) | XP_006717067.1:p.Val180= | |
| XM_011518365.1:c.540G>A (FANCC) | XP_011516667.1:p.Val180= | |
| XM_011518366.1:c.540G>A (FANCC) | XP_011516668.1:p.Val180= | |
| XM_011518367.1:c.84G>A (FANCC) | XP_011516669.1:p.Val28= | |
| XM_006717001.3:c.522-14567G>A (FANCC) | XP_006717064.1:n.522-14567G>A | |
| XM_006717002.4:c.540G>A (FANCC) | XP_006717065.1:p.Val180= | |
| XM_006717004.4:c.540G>A (FANCC) | XP_006717067.1:p.Val180= | |
| XM_011518365.3:c.540G>A (FANCC) | XP_011516667.1:p.Val180= | |
| XM_011518366.3:c.540G>A (FANCC) | XP_011516668.1:p.Val180= | |
| XM_011518367.2:c.84G>A (FANCC) | XP_011516669.1:p.Val28= | |
| XM_017014452.2:c.84G>A (FANCC) | XP_016869941.1:p.Val28= | |
| XM_017014453.1:c.84G>A (FANCC) | XP_016869942.1:p.Val28= | |
| XM_017014454.1:c.66-14567G>A (FANCC) | XP_016869943.1:n.66-14567G>A | |
| XM_024447451.1:c.540G>A (FANCC) | XP_024303219.1:p.Val180= | |
| NM_000136.3:c.540G>A (FANCC) MANE Select | NP_000127.2:p.Val180= | |
| NM_001243743.2:c.540G>A (FANCC) | NP_001230672.1:p.Val180= | |
| NM_001243744.2:c.540G>A (FANCC) | NP_001230673.1:p.Val180= |