HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071675T>C , CM000667.2:g.111071675T>C | GRCh38 |
NC_000005.9:g.110407373T>C , CM000667.1:g.110407373T>C | GRCh37 |
NC_000005.8:g.110435272T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000420978.6:c.34+158T>C | ENSP00000399099.2:n.34+158T>C | |
NR_045089.1:n.1438+158T>C | ||
NR_045089.2:n.1456+158T>C |