Linked Data
gnomAD v4:
12-52814170-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814170T>C , CM000674.2:g.52814170T>C | GRCh38 |
| NC_000012.11:g.53207954T>C , CM000674.1:g.53207954T>C | GRCh37 |
| NC_000012.10:g.51494221T>C | NCBI36 |
| NG_007380.1:g.5382A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.1:c.-112A>G | ENSP00000448220.1:n.-112A>G |