Linked Data
gnomAD v4:
11-119093552-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119093552T>C , CM000673.2:g.119093552T>C | GRCh38 |
| NC_000011.9:g.118964262T>C , CM000673.1:g.118964262T>C | GRCh37 |
| NC_000011.8:g.118469472T>C | NCBI36 |
| NG_008093.1:g.13676T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686218.1:c.*269T>C | ENSP00000509288.1:n.*269T>C |