Linked Data
gnomAD v4:
5-111071572-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071573dup , CM000667.2:g.111071573dup | GRCh38 |
| NC_000005.9:g.110407271dup , CM000667.1:g.110407271dup | GRCh37 |
| NC_000005.8:g.110435170dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420978.6:c.34+56dup | ENSP00000399099.2:n.34+56dup | |
| NR_045089.1:n.1438+56dup | ||
| NR_045089.2:n.1456+56dup |