HGVS | Genome Assembly |
---|---|
NC_000005.10:g.151622092C>A , CM000667.2:g.151622092C>A | GRCh38 |
NC_000005.9:g.151001653C>A , CM000667.1:g.151001653C>A | GRCh37 |
NC_000005.8:g.150981846C>A | NCBI36 |
NG_046979.1:g.35049G>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011537598.1:c.-350+19230G>T | XP_011535900.1:n.-350+19230G>T | |
XM_011537599.1:c.-543+19230G>T | XP_011535901.1:n.-543+19230G>T | |
XM_011537602.1:c.-194+19230G>T | XP_011535904.1:n.-194+19230G>T | |
XM_011537604.1:c.-350+19230G>T | XP_011535906.1:n.-350+19230G>T | |
XM_011537605.1:c.-350+19230G>T | XP_011535907.1:n.-350+19230G>T | |
XM_011537606.1:c.-350+19230G>T | XP_011535908.1:n.-350+19230G>T | |
XR_944310.1:n.214+19230G>T |