HGVS | Genome Assembly |
---|---|
NC_000016.10:g.73547159A>G , CM000678.2:g.73547159A>G | GRCh38 |
NC_000016.9:g.73581058A>G , CM000678.1:g.73581058A>G | GRCh37 |
NC_000016.8:g.72138559A>G | NCBI36 |
NG_013211.2:g.349773T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000641206.2:c.-1546-90901T>C | ENSP00000493252.1:n.-1546-90901T>C | |
XM_024450275.1:c.-493-90901T>C | XP_024306043.1:n.-493-90901T>C | |
NM_001386735.1:c.-1063-90901T>C | NP_001373664.1:n.-1063-90901T>C |