Linked Data
gnomAD v4:
17-39665249-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665249T>G , CM000679.2:g.39665249T>G | GRCh38 |
| NC_000017.10:g.37821502T>G , CM000679.1:g.37821502T>G | GRCh37 |
| NC_000017.9:g.35075028T>G | NCBI36 |
| NG_008892.1:g.4904T>G , LRG_210:g.4904T>G | |
| NG_042278.1:g.2269T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.2:c.-111T>G | ENSP00000312624.2:n.-111T>G |