Linked Data
gnomAD v4:
1-207454195-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207454195T>C , CM000663.2:g.207454195T>C | GRCh38 |
| NC_000001.10:g.207627540T>C , CM000663.1:g.207627540T>C | GRCh37 |
| NC_000001.9:g.205694163T>C | NCBI36 |
| NG_013006.1:g.4896T>C , LRG_348:g.4896T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699640.1:c.-385+1100T>C | ENSP00000514493.1:n.-385+1100T>C |