Linked Data
gnomAD v4:
17-39665294-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665294C>T , CM000679.2:g.39665294C>T | GRCh38 |
| NC_000017.10:g.37821547C>T , CM000679.1:g.37821547C>T | GRCh37 |
| NC_000017.9:g.35075073C>T | NCBI36 |
| NG_008892.1:g.4949C>T , LRG_210:g.4949C>T | |
| NG_042278.1:g.2314C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.2:c.-66C>T | ENSP00000312624.2:n.-66C>T |