HGVS | Genome Assembly |
---|---|
NC_000002.12:g.168901052G>A , CM000664.2:g.168901052G>A | GRCh38 |
NC_000002.11:g.169757562G>A , CM000664.1:g.169757562G>A | GRCh37 |
NC_000002.10:g.169465808G>A | NCBI36 |
NG_011682.1:g.4813G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000451987.5:c.-172-10366C>T | ENSP00000393322.1:n.-172-10366C>T | |
ENST00000472216.2:n.177-10366C>T |