Linked Data
gnomAD v4:
17-74920195-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920195G>C , CM000679.2:g.74920195G>C | GRCh38 |
| NC_000017.10:g.72916290G>C , CM000679.1:g.72916290G>C | GRCh37 |
| NC_000017.9:g.70427885G>C | NCBI36 |
| NG_007882.1:g.8062C>G | |
| NG_033062.1:g.921G>C | |
| NG_007882.2:g.8069C>G | |
| NG_033062.2:g.921G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.641C>G MANE Select | ENSP00000480279.1:p.Thr214Ser | |
| ENST00000579243.1:c.*240C>G | ENSP00000462568.1:n.*240C>G | |
| ENST00000614341.4:c.641C>G | ENSP00000480279.1:p.Thr214Ser | |
| NM_001282489.2:c.332C>G | NP_001269418.1:p.Thr111Ser | |
| NM_173477.4:c.641C>G | NP_775748.2:p.Thr214Ser | |
| XM_011524296.1:c.332C>G | XP_011522598.1:p.Thr111Ser | |
| XM_011524296.2:c.332C>G | XP_011522598.1:p.Thr111Ser | |
| NM_173477.5:c.641C>G MANE Select | NP_775748.2:p.Thr214Ser | |
| NM_001282489.3:c.332C>G | NP_001269418.1:p.Thr111Ser |