Linked Data
gnomAD v4:
11-113475416-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.113475416C>T , CM000673.2:g.113475416C>T | GRCh38 |
| NC_000011.9:g.113346138C>T , CM000673.1:g.113346138C>T | GRCh37 |
| NC_000011.8:g.112851348C>T | NCBI36 |
| NG_008841.1:g.4864G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000540600.5:n.34+242G>A |