Linked Data
ClinVar Variation Id:
1749282
ClinVar RCV Id:
RCV002347682
dbSNP Id:
rs1338032715
gnomAD v3:
11-116790658-A-T
gnomAD v4:
11-116790658-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116790658A>T , CM000673.2:g.116790658A>T | GRCh38 |
| NC_000011.9:g.116661374A>T , CM000673.1:g.116661374A>T | GRCh37 |
| NC_000011.8:g.116166584A>T | NCBI36 |
| NG_015894.1:g.6763T>A | |
| NG_015894.2:g.6763T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227665.9:c.571T>A MANE Select | ENSP00000227665.4:p.Phe191Ile | |
| ENST00000433069.2:c.571T>A | ENSP00000399701.2:p.Phe191Ile | |
| ENST00000673688.1:c.655T>A | ENSP00000501141.1:p.Phe219Ile | |
| ENST00000227665.8:c.571T>A | ENSP00000227665.4:p.Phe191Ile | |
| ENST00000542499.5:c.571T>A | ENSP00000445002.1:p.Phe191Ile | |
| NM_001166598.1:c.571T>A | NP_001160070.1:p.Phe191Ile | |
| NM_052968.4:c.571T>A | NP_443200.2:p.Phe191Ile | |
| NM_001166598.2:c.571T>A | NP_001160070.1:p.Phe191Ile | |
| NM_001371904.1:c.571T>A MANE Select | NP_001358833.1:p.Phe191Ile | |
| NM_052968.5:c.571T>A | NP_443200.2:p.Phe191Ile |