HGVS | Genome Assembly |
---|---|
NC_000010.11:g.55031247C>T , CM000672.2:g.55031247C>T | GRCh38 |
NC_000010.10:g.56791007C>T , CM000672.1:g.56791007C>T | GRCh37 |
NC_000010.9:g.56461013C>T | NCBI36 |
NG_009191.3:g.602936G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000458638.1:c.-79-133747G>A | ENSP00000394465.1:n.-79-133747G>A | |
ENST00000613346.4:c.-79-133747G>A | ENSP00000481211.1:n.-79-133747G>A | |
NM_001354404.1:c.-79-133747G>A | NP_001341333.1:n.-79-133747G>A | |
XM_017016573.2:c.-156-82646G>A | XP_016872062.1:n.-156-82646G>A | |
NM_001354404.2:c.-79-133747G>A | NP_001341333.1:n.-79-133747G>A |