Linked Data
gnomAD v4:
17-8075709-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075709T>C , CM000679.2:g.8075709T>C | GRCh38 |
| NC_000017.10:g.7979027T>C , CM000679.1:g.7979027T>C | GRCh37 |
| NC_000017.9:g.7919752T>C | NCBI36 |
| NG_007099.1:g.16995A>G | |
| NG_007099.2:g.17008A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1540A>G MANE Select | ENSP00000497784.1:p.Thr514Ala | |
| ENST00000649809.1:c.604A>G | ENSP00000496845.1:p.Thr202Ala | |
| ENST00000319144.4:c.1540A>G | ENSP00000315167.4:p.Thr514Ala | |
| ENST00000577351.5:n.479+466A>G | ||
| NM_001139.2:c.1540A>G | NP_001130.1:p.Thr514Ala | |
| NM_001139.3:c.1540A>G MANE Select | NP_001130.1:p.Thr514Ala |