HGVS | Genome Assembly |
---|---|
NC_000003.12:g.114232449C>T , CM000665.2:g.114232449C>T | GRCh38 |
NC_000003.11:g.113951296C>T , CM000665.1:g.113951296C>T | GRCh37 |
NC_000003.10:g.115433986C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000473625.1:n.573G>A | ||
XR_001740856.1:n.161-893C>T |