Linked Data
ClinVar Variation Id:
2727268
ClinVar RCV Id:
RCV003524908
dbSNP Id:
rs776210193
gnomAD v4:
3-10087167-A-G
MyVariant Identifiers:
chr3:g.10128851A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10087167A>G , CM000665.2:g.10087167A>G | GRCh38 |
| NC_000003.11:g.10128851A>G , CM000665.1:g.10128851A>G | GRCh37 |
| NC_000003.10:g.10103851A>G | NCBI36 |
| NG_007311.1:g.65739A>G , LRG_306:g.65739A>G | |
| NG_042053.1:g.26065T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681997.1:n.2453A>G (FANCD2) | ||
| ENST00000683263.1:n.2368A>G (FANCD2) | ||
| ENST00000683933.1:n.264-1282A>G (FANCD2) | ||
| ENST00000675286.1:c.3369A>G (FANCD2) MANE Select | ENSP00000502379.1:p.Gln1123= | |
| ENST00000676013.1:c.3258A>G (FANCD2) | ENSP00000501999.1:p.Gln1086= | |
| ENST00000287647.7:c.3369A>G (FANCD2) | ENSP00000287647.3:p.Gln1123= | |
| ENST00000383807.5:c.3369A>G (FANCD2) | ENSP00000373318.1:p.Gln1123= | |
| ENST00000419585.5:c.3369A>G (FANCD2) | ENSP00000398754.1:p.Gln1123= | |
| ENST00000421731.5:c.1868A>G (FANCD2) | ||
| ENST00000431315.5:n.169T>C (FANCD2OS) | ||
| ENST00000436517.5:n.190T>C (FANCD2OS) | ||
| ENST00000524279.1:c.*44-5636T>C (FANCD2OS) | ENSP00000429663.1:n.*44-5636T>C | |
| NM_001018115.1:c.3369A>G , LRG_306t1:c.3369A>G (FANCD2) | NP_001018125.1:p.Gln1123= | |
| NM_033084.3:c.3369A>G , LRG_306t2:c.3369A>G (FANCD2) | NP_149075.2:p.Gln1123= | |
| NM_173472.1:c.*44-5636T>C (FANCD2OS) | NP_775743.1:n.*44-5636T>C | |
| XM_005264946.2:c.3369A>G (FANCD2) | XP_005265003.1:p.Gln1123= | |
| XM_005264947.2:c.1374A>G (FANCD2) | XP_005265004.1:p.Gln458= | |
| XM_006713021.2:c.3369A>G (FANCD2) | XP_006713084.1:p.Gln1123= | |
| XM_006713023.2:c.3369A>G (FANCD2) | XP_006713086.1:p.Gln1123= | |
| XM_006713024.2:c.3252A>G (FANCD2) | XP_006713087.1:p.Gln1084= | |
| XM_011533479.1:c.3369A>G (FANCD2) | XP_011531781.1:p.Gln1123= | |
| XM_011533480.1:c.2220A>G (FANCD2) | XP_011531782.1:p.Gln740= | |
| NM_001018115.2:c.3369A>G (FANCD2) | NP_001018125.1:p.Gln1123= | |
| NM_001319984.1:c.3369A>G (FANCD2) | NP_001306913.1:p.Gln1123= | |
| NM_033084.4:c.3369A>G (FANCD2) | NP_149075.2:p.Gln1123= | |
| NM_001018115.3:c.3369A>G (FANCD2) MANE Select | NP_001018125.1:p.Gln1123= | |
| NM_001319984.2:c.3369A>G (FANCD2) | NP_001306913.1:p.Gln1123= | |
| NM_001374253.1:c.3258A>G (FANCD2) | NP_001361182.1:p.Gln1086= | |
| NM_001374254.1:c.3369A>G (FANCD2) | NP_001361183.1:p.Gln1123= | |
| NM_033084.6:c.3369A>G (FANCD2) | NP_149075.2:p.Gln1123= | |
| NM_173472.2:c.*44-5636T>C (FANCD2OS) | NP_775743.1:n.*44-5636T>C |