HGVS | Genome Assembly |
---|---|
NC_000004.12:g.35981447G>A , CM000666.2:g.35981447G>A | GRCh38 |
NC_000004.11:g.35983069G>A , CM000666.1:g.35983069G>A | GRCh37 |
NC_000004.10:g.35659464G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000503225.5:n.1607+3783C>T | ||
XR_925192.1:n.1502C>T |