Linked Data
gnomAD v4:
17-7668308-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7668308C>T , CM000679.2:g.7668308C>T | GRCh38 |
| NC_000017.10:g.7571626C>T , CM000679.1:g.7571626C>T | GRCh37 |
| NC_000017.9:g.7512351C>T | NCBI36 |
| NG_017013.2:g.24243G>A , LRG_321:g.24243G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000359597.8:c.994-2064G>A | ENSP00000352610.4:n.994-2064G>A | |
| ENST00000413465.6:c.782+5873G>A | ENSP00000410739.2:n.782+5873G>A | |
| ENST00000635293.1:c.984-883G>A | ENSP00000488924.1:n.984-883G>A |