HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652636_171652637insACA , CM000663.2:g.171652636_171652637insACA | GRCh38 |
NC_000001.10:g.171621776_171621777insACA , CM000663.1:g.171621776_171621777insACA | GRCh37 |
NC_000001.9:g.169888399_169888400insACA | NCBI36 |
NG_008859.1:g.4997_4998insTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-26_-25insTGT MANE Select | ENSP00000037502.5:n.-26_-25insTGT | |
ENST00000037502.10:c.-26_-25insTGT | ENSP00000037502.5:n.-26_-25insTGT | |
NM_000261.2:c.-26_-25insTGT MANE Select | NP_000252.1:n.-26_-25insTGT |