HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150832322G>T , CM000669.2:g.150832322G>T | GRCh38 |
NC_000007.13:g.150529410G>T , CM000669.1:g.150529410G>T | GRCh37 |
NC_000007.12:g.150160343G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467291.5:c.-93+4920G>T | ENSP00000418328.1:n.-93+4920G>T | |
ENST00000493429.5:c.-93+4920G>T | ENSP00000418614.1:n.-93+4920G>T | |
XM_011516008.1:c.-182+4920G>T | XP_011514310.1:n.-182+4920G>T | |
XR_928169.1:n.352-3414C>A | ||
XR_928170.1:n.482-3414C>A | ||
XR_928171.1:n.354-3414C>A | ||
XM_017011944.1:c.-93+4920G>T | XP_016867433.1:n.-93+4920G>T | |
XM_017011945.1:c.-93+4920G>T | XP_016867434.1:n.-93+4920G>T | |
XR_928169.2:n.358-3414C>A | ||
XR_928171.2:n.358-3414C>A |