Linked Data
gnomAD v4:
17-74920177-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920177A>G , CM000679.2:g.74920177A>G | GRCh38 |
| NC_000017.10:g.72916272A>G , CM000679.1:g.72916272A>G | GRCh37 |
| NC_000017.9:g.70427867A>G | NCBI36 |
| NG_007882.1:g.8080T>C | |
| NG_033062.1:g.903A>G | |
| NG_007882.2:g.8087T>C | |
| NG_033062.2:g.903A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.659T>C MANE Select | ENSP00000480279.1:p.Leu220Pro | |
| ENST00000579243.1:c.*258T>C | ENSP00000462568.1:n.*258T>C | |
| ENST00000614341.4:c.659T>C | ENSP00000480279.1:p.Leu220Pro | |
| NM_001282489.2:c.350T>C | NP_001269418.1:p.Leu117Pro | |
| NM_173477.4:c.659T>C | NP_775748.2:p.Leu220Pro | |
| XM_011524296.1:c.350T>C | XP_011522598.1:p.Leu117Pro | |
| XM_011524296.2:c.350T>C | XP_011522598.1:p.Leu117Pro | |
| NM_173477.5:c.659T>C MANE Select | NP_775748.2:p.Leu220Pro | |
| NM_001282489.3:c.350T>C | NP_001269418.1:p.Leu117Pro |