Linked Data
gnomAD v4:
17-39665252-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665252C>A , CM000679.2:g.39665252C>A | GRCh38 |
| NC_000017.10:g.37821505C>A , CM000679.1:g.37821505C>A | GRCh37 |
| NC_000017.9:g.35075031C>A | NCBI36 |
| NG_008892.1:g.4907C>A , LRG_210:g.4907C>A | |
| NG_042278.1:g.2272C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.2:c.-108C>A | ENSP00000312624.2:n.-108C>A |