Linked Data
gnomAD v4:
17-66228076-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228076C>G , CM000679.2:g.66228076C>G | GRCh38 |
| NC_000017.10:g.64224194C>G , CM000679.1:g.64224194C>G | GRCh37 |
| NC_000017.9:g.61654656C>G | NCBI36 |
| NG_012045.1:g.6363G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.185G>C MANE Select | ENSP00000205948.6:p.Arg62Thr | |
| ENST00000205948.10:c.185G>C | ENSP00000205948.6:p.Arg62Thr | |
| ENST00000577982.1:c.185G>C | ENSP00000464301.1:p.Arg62Thr | |
| ENST00000581797.5:c.5G>C | ENSP00000463553.1:p.Arg2Thr | |
| NM_000042.2:c.185G>C | NP_000033.2:p.Arg62Thr | |
| NM_000042.3:c.185G>C MANE Select | NP_000033.2:p.Arg62Thr |