HGVS | Genome Assembly |
---|---|
NC_000001.11:g.220837171T>A , CM000663.2:g.220837171T>A | GRCh38 |
NC_000001.10:g.221010513T>A , CM000663.1:g.221010513T>A | GRCh37 |
NC_000001.9:g.219077136T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651706.1:c.842+31897T>A | ENSP00000499157.1:n.842+31897T>A | |
NR_046901.1:n.293-3979A>T |