HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92419018A>T , CM000672.2:g.92419018A>T | GRCh38 |
NC_000010.10:g.94178775A>T , CM000672.1:g.94178775A>T | GRCh37 |
NC_000010.9:g.94168755A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000430958.1:n.352A>T | ||
NR_038243.2:n.358A>T |