HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127080131T>C , CM000670.2:g.127080131T>C | GRCh38 |
NC_000008.10:g.128092376T>C , CM000670.1:g.128092376T>C | GRCh37 |
NC_000008.9:g.128161558T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_109833.1:n.258T>C (PRNCR1) | ||
NR_119373.1:n.102-998A>G (PCAT2) |