Linked Data
gnomAD v4:
1-186680518-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680518C>T , CM000663.2:g.186680518C>T | GRCh38 |
| NC_000001.10:g.186649650C>T , CM000663.1:g.186649650C>T | GRCh37 |
| NC_000001.9:g.184916273C>T | NCBI36 |
| NG_028206.2:g.4910G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-113-115G>A | ENSP00000506242.1:n.-113-115G>A |