HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99144369T>A , CM000666.2:g.99144369T>A | GRCh38 |
NC_000004.11:g.100065520T>A , CM000666.1:g.100065520T>A | GRCh37 |
NC_000004.10:g.100284543T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000504581.1:n.170-1589A>T | ||
NR_037884.1:n.680-10176T>A |