HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127080211T>G , CM000670.2:g.127080211T>G | GRCh38 |
NC_000008.10:g.128092456T>G , CM000670.1:g.128092456T>G | GRCh37 |
NC_000008.9:g.128161638T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_109833.1:n.338T>G (PRNCR1) | ||
NR_119373.1:n.102-1078A>C (PCAT2) |