HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127080248T>C , CM000670.2:g.127080248T>C | GRCh38 |
NC_000008.10:g.128092493T>C , CM000670.1:g.128092493T>C | GRCh37 |
NC_000008.9:g.128161675T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_109833.1:n.375T>C (PRNCR1) | ||
NR_119373.1:n.102-1115A>G (PCAT2) |