Linked Data
gnomAD v4:
5-111071666-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071666C>T , CM000667.2:g.111071666C>T | GRCh38 |
| NC_000005.9:g.110407364C>T , CM000667.1:g.110407364C>T | GRCh37 |
| NC_000005.8:g.110435263C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420978.6:c.34+149C>T | ENSP00000399099.2:n.34+149C>T | |
| NR_045089.1:n.1438+149C>T | ||
| NR_045089.2:n.1456+149C>T |