Linked Data
ClinVar Variation Id:
2614266
ClinVar RCV Id:
RCV003376485
dbSNP Id:
rs1052799986
gnomAD v4:
3-142562978-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142562978A>C , CM000665.2:g.142562978A>C | GRCh38 |
| NC_000003.11:g.142281820A>C , CM000665.1:g.142281820A>C | GRCh37 |
| NC_000003.10:g.143764510A>C | NCBI36 |
| NG_008951.1:g.20849T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350721.9:c.424T>G MANE Select | ENSP00000343741.4:p.Phe142Val | |
| ENST00000515149.3:c.293-1557T>G | ENSP00000425897.3:n.293-1557T>G | |
| ENST00000653868.1:n.453T>G | ||
| ENST00000657914.1:n.2782T>G | ||
| ENST00000659195.1:n.2489T>G | ||
| ENST00000661310.1:c.424T>G | ENSP00000499589.1:p.Phe142Val | |
| ENST00000350721.8:c.424T>G | ENSP00000343741.4:p.Phe142Val | |
| ENST00000507148.1:c.293-630T>G | ENSP00000426595.1:n.293-630T>G | |
| NM_001184.3:c.424T>G | NP_001175.2:p.Phe142Val | |
| XM_011512924.1:c.424T>G | XP_011511226.1:p.Phe142Val | |
| XM_011512925.1:c.424T>G | XP_011511227.1:p.Phe142Val | |
| XM_011512926.1:c.424T>G | XP_011511228.1:p.Phe142Val | |
| XM_011512927.1:c.424T>G | XP_011511229.1:p.Phe142Val | |
| XR_924147.1:n.513T>G | ||
| XR_924148.1:n.513T>G | ||
| XR_924149.1:n.513T>G | ||
| NM_001354579.1:c.424T>G | NP_001341508.1:p.Phe142Val | |
| XR_001740179.2:n.513T>G | ||
| XR_001740180.2:n.513T>G | ||
| XR_001740181.2:n.513T>G | ||
| XR_001740182.1:n.513T>G | ||
| XR_002959543.1:n.513T>G | ||
| XR_924148.2:n.513T>G | ||
| NM_001184.4:c.424T>G MANE Select | NP_001175.2:p.Phe142Val | |
| NM_001354579.2:c.424T>G | NP_001341508.1:p.Phe142Val |