Linked Data
gnomAD v4:
17-34255220-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255220T>C , CM000679.2:g.34255220T>C | GRCh38 |
| NC_000017.10:g.32582239T>C , CM000679.1:g.32582239T>C | GRCh37 |
| NC_000017.9:g.29606352T>C | NCBI36 |
| NG_012123.1:g.4944T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624362.1:n.3T>C |