HGVS | Genome Assembly |
---|---|
NC_000010.11:g.55089142A>G , CM000672.2:g.55089142A>G | GRCh38 |
NC_000010.10:g.56848902A>G , CM000672.1:g.56848902A>G | GRCh37 |
NC_000010.9:g.56518908A>G | NCBI36 |
NG_009191.3:g.545041T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000458638.1:c.-80+77434T>C | ENSP00000394465.1:n.-80+77434T>C | |
ENST00000613346.4:c.-80+77434T>C | ENSP00000481211.1:n.-80+77434T>C | |
NM_001354404.1:c.-80+77434T>C | NP_001341333.1:n.-80+77434T>C | |
XM_017016573.2:c.-157+77434T>C | XP_016872062.1:n.-157+77434T>C | |
NM_001354404.2:c.-80+77434T>C | NP_001341333.1:n.-80+77434T>C |