HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071615T>C , CM000667.2:g.111071615T>C | GRCh38 |
NC_000005.9:g.110407313T>C , CM000667.1:g.110407313T>C | GRCh37 |
NC_000005.8:g.110435212T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000420978.6:c.34+98T>C | ENSP00000399099.2:n.34+98T>C | |
NR_045089.1:n.1438+98T>C | ||
NR_045089.2:n.1456+98T>C |