Linked Data
gnomAD v4:
11-113475540-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.113475540G>T , CM000673.2:g.113475540G>T | GRCh38 |
| NC_000011.9:g.113346262G>T , CM000673.1:g.113346262G>T | GRCh37 |
| NC_000011.8:g.112851472G>T | NCBI36 |
| NG_008841.1:g.4740C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000540600.5:n.34+118C>A | ||
| XR_948024.2:n.902C>A |