Linked Data
gnomAD v4:
17-74920211-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920211T>C , CM000679.2:g.74920211T>C | GRCh38 |
| NC_000017.10:g.72916306T>C , CM000679.1:g.72916306T>C | GRCh37 |
| NC_000017.9:g.70427901T>C | NCBI36 |
| NG_007882.1:g.8046A>G | |
| NG_033062.1:g.937T>C | |
| NG_007882.2:g.8053A>G | |
| NG_033062.2:g.937T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.625A>G MANE Select | ENSP00000480279.1:p.Thr209Ala | |
| ENST00000579243.1:c.*224A>G | ENSP00000462568.1:n.*224A>G | |
| ENST00000614341.4:c.625A>G | ENSP00000480279.1:p.Thr209Ala | |
| NM_001282489.2:c.316A>G | NP_001269418.1:p.Thr106Ala | |
| NM_173477.4:c.625A>G | NP_775748.2:p.Thr209Ala | |
| XM_011524296.1:c.316A>G | XP_011522598.1:p.Thr106Ala | |
| XM_011524296.2:c.316A>G | XP_011522598.1:p.Thr106Ala | |
| NM_173477.5:c.625A>G MANE Select | NP_775748.2:p.Thr209Ala | |
| NM_001282489.3:c.316A>G | NP_001269418.1:p.Thr106Ala |