Linked Data
ClinVar Variation Id:
456128
dbSNP Id:
rs368506826
ExAC:
16:89805125 G / C
gnomAD v2:
16-89805125-G-C
gnomAD v3:
16-89738717-G-C
gnomAD v4:
16-89738717-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89738717G>C , CM000678.2:g.89738717G>C | GRCh38 |
| NC_000016.9:g.89805125G>C , CM000678.1:g.89805125G>C | GRCh37 |
| NC_000016.8:g.88332626G>C | NCBI36 |
| NG_011706.1:g.82941C>G , LRG_495:g.82941C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2998C>G (FANCA) | ENSP00000512522.1:n.*2998C>G | |
| ENST00000564475.6:c.*37C>G (FANCA) | ENSP00000454977.2:n.*37C>G | |
| ENST00000567510.2:c.2835-9C>G (FANCA) | ENSP00000455969.1:n.2835-9C>G | |
| ENST00000568369.6:c.4265-9C>G (FANCA) | ENSP00000456829.1:n.4265-9C>G | |
| ENST00000696274.1:n.4386C>G (FANCA) | ||
| ENST00000696275.1:c.*3664C>G (FANCA) | ENSP00000512517.1:n.*3664C>G | |
| ENST00000696286.1:c.*174-9C>G (FANCA) | ENSP00000512523.1:n.*174-9C>G | |
| ENST00000696287.1:c.*37C>G (FANCA) | ENSP00000512524.1:n.*37C>G | |
| ENST00000696291.1:c.*3857C>G (FANCA) | ENSP00000512530.1:n.*3857C>G | |
| ENST00000389301.8:c.4261-9C>G (FANCA) MANE Select | ENSP00000373952.3:n.4261-9C>G | |
| ENST00000443381.7:c.*471G>C (ZNF276) MANE Select | ENSP00000415836.2:n.*471G>C | |
| ENST00000289816.9:c.*471G>C (ZNF276) | ENSP00000289816.5:n.*471G>C | |
| ENST00000389301.7:c.4261-9C>G (FANCA) | ENSP00000373952.3:n.4261-9C>G | |
| ENST00000561722.5:c.481-9C>G (FANCA) | ENSP00000456608.1:n.481-9C>G | |
| ENST00000562424.1:n.532-9C>G (FANCA) | ||
| ENST00000563983.5:n.2304G>C (ZNF276) | ||
| ENST00000567879.5:c.635-9C>G (FANCA) | ENSP00000457006.1:n.635-9C>G | |
| ENST00000568369.5:c.4265-9C>G (FANCA) | ENSP00000456829.1:n.4265-9C>G | |
| NM_000135.2:c.4261-9C>G , LRG_495t1:c.4261-9C>G (FANCA) | NP_000126.2:n.4261-9C>G | |
| NM_001113525.1:c.*471G>C (ZNF276) | NP_001106997.1:n.*471G>C | |
| NM_001286167.1:c.4265-9C>G (FANCA) | NP_001273096.1:n.4265-9C>G | |
| NM_152287.3:c.*471G>C (ZNF276) | NP_689500.2:n.*471G>C | |
| NR_110122.1:n.2488G>C (ZNF276) | ||
| NR_110126.1:n.2371G>C (ZNF276) | ||
| NR_110128.1:n.2294G>C (ZNF276) | ||
| NR_110129.1:n.2383G>C (ZNF276) | ||
| XR_933244.1:n.4228-9C>G (FANCA) | ||
| XR_933245.1:n.4165-9C>G (FANCA) | ||
| NM_000135.3:c.4261-9C>G (FANCA) | NP_000126.2:n.4261-9C>G | |
| NM_001286167.2:c.4265-9C>G (FANCA) | NP_001273096.1:n.4265-9C>G | |
| XM_005256294.4:c.*37C>G (FANCA) | XP_005256351.1:n.*37C>G | |
| XM_011522945.2:c.*37C>G (FANCA) | XP_011521247.1:n.*37C>G | |
| XM_011522946.3:c.*37C>G (FANCA) | XP_011521248.1:n.*37C>G | |
| XM_011522947.2:c.*37C>G (FANCA) | XP_011521249.1:n.*37C>G | |
| XM_017023044.2:c.4132-9C>G (FANCA) | XP_016878533.1:n.4132-9C>G | |
| XM_017023890.1:c.*471G>C (ZNF276) | XP_016879379.1:n.*471G>C | |
| XM_024450189.1:c.*37C>G (FANCA) | XP_024305957.1:n.*37C>G | |
| XR_933244.2:n.4228-9C>G (FANCA) | ||
| XR_933245.2:n.4165-9C>G (FANCA) | ||
| XR_933484.2:n.2482G>C (ZNF276) | ||
| NM_000135.4:c.4261-9C>G (FANCA) MANE Select | NP_000126.2:n.4261-9C>G | |
| NM_001113525.2:c.*471G>C (ZNF276) MANE Select | NP_001106997.1:n.*471G>C | |
| NM_001286167.3:c.4265-9C>G (FANCA) | NP_001273096.1:n.4265-9C>G | |
| NM_152287.4:c.*471G>C (ZNF276) | NP_689500.2:n.*471G>C | |
| NR_110122.2:n.2471G>C (ZNF276) | ||
| NR_110126.2:n.2354G>C (ZNF276) | ||
| NR_110129.2:n.2388G>C (ZNF276) | ||
| NR_110128.2:n.2294G>C (ZNF276) |