Linked Data
gnomAD v4:
17-35880696-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35880696A>G , CM000679.2:g.35880696A>G | GRCh38 |
| NC_000017.9:g.31231813A>G | NCBI36 |
| NG_015990.1:g.4678T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000605509.2:c.-18+33T>C | ENSP00000474141.2:n.-18+33T>C | |
| ENST00000605140.5:c.-18+33T>C | ENSP00000475057.1:n.-18+33T>C | |
| XR_934696.1:n.197-3686A>G | ||
| XR_934697.1:n.200-3686A>G | ||
| XR_001752852.1:n.426+622A>G | ||
| XR_934696.2:n.91-3686A>G | ||
| XR_934697.2:n.91-3686A>G |