HGVS | Genome Assembly |
---|---|
NC_000010.11:g.54901702A>G , CM000672.2:g.54901702A>G | GRCh38 |
NC_000010.10:g.56661462A>G , CM000672.1:g.56661462A>G | GRCh37 |
NC_000010.9:g.56331468A>G | NCBI36 |
NG_009191.3:g.732481T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000458638.1:c.-79-4202T>C | ENSP00000394465.1:n.-79-4202T>C | |
ENST00000613346.4:c.-79-4202T>C | ENSP00000481211.1:n.-79-4202T>C | |
NM_001354404.1:c.-79-4202T>C | NP_001341333.1:n.-79-4202T>C | |
XM_017016573.2:c.-79-4202T>C | XP_016872062.1:n.-79-4202T>C | |
NM_001354404.2:c.-79-4202T>C | NP_001341333.1:n.-79-4202T>C |