Linked Data
gnomAD v4:
1-186680522-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186680522T>G , CM000663.2:g.186680522T>G | GRCh38 |
| NC_000001.10:g.186649654T>G , CM000663.1:g.186649654T>G | GRCh37 |
| NC_000001.9:g.184916277T>G | NCBI36 |
| NG_028206.2:g.4906A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680451.1:c.-113-119A>C | ENSP00000506242.1:n.-113-119A>C |