HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32164213_32164214insA , CM000668.2:g.32164213_32164214insA | GRCh38 |
NC_000006.11:g.32131990_32131991insA , CM000668.1:g.32131990_32131991insA | GRCh37 |
NC_000006.10:g.32239968_32239969insA | NCBI36 |
NG_042283.1:g.15762_15763insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000421600.2:c.225-366_225-365insA | ||
ENST00000422437.5:c.766-366_766-365insA | ENSP00000457534.1:n.766-366_766-365insA | |
ENST00000428388.6:c.766-366_766-365insA | ENSP00000455087.1:n.766-366_766-365insA | |
ENST00000453656.6:n.897-366_897-365insA | ||
ENST00000479001.2:n.751-366_751-365insA | ||
ENST00000583227.5:c.*318-366_*318-365insA | ENSP00000461909.1:n.*318-366_*318-365insA | |
ENST00000585246.5:c.*317+1591_*317+1592insA | ENSP00000463570.1:n.*317+1591_*317+1592insA | |
NR_037861.1:n.1180-366_1180-365insA |