HGVS | Genome Assembly |
---|---|
NC_000010.11:g.55089120T>C , CM000672.2:g.55089120T>C | GRCh38 |
NC_000010.10:g.56848880T>C , CM000672.1:g.56848880T>C | GRCh37 |
NC_000010.9:g.56518886T>C | NCBI36 |
NG_009191.3:g.545063A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000458638.1:c.-80+77456A>G | ENSP00000394465.1:n.-80+77456A>G | |
ENST00000613346.4:c.-80+77456A>G | ENSP00000481211.1:n.-80+77456A>G | |
NM_001354404.1:c.-80+77456A>G | NP_001341333.1:n.-80+77456A>G | |
XM_017016573.2:c.-157+77456A>G | XP_016872062.1:n.-157+77456A>G | |
NM_001354404.2:c.-80+77456A>G | NP_001341333.1:n.-80+77456A>G |