Linked Data
gnomAD v4:
17-39665098-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665098G>T , CM000679.2:g.39665098G>T | GRCh38 |
| NC_000017.10:g.37821351G>T , CM000679.1:g.37821351G>T | GRCh37 |
| NC_000017.9:g.35074877G>T | NCBI36 |
| NG_008892.1:g.4753G>T , LRG_210:g.4753G>T | |
| NG_042278.1:g.2118G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.2:c.-262G>T | ENSP00000312624.2:n.-262G>T |