HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127080210C>T , CM000670.2:g.127080210C>T | GRCh38 |
NC_000008.10:g.128092455C>T , CM000670.1:g.128092455C>T | GRCh37 |
NC_000008.9:g.128161637C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_109833.1:n.337C>T (PRNCR1) | ||
NR_119373.1:n.102-1077G>A (PCAT2) |