HGVS | Genome Assembly |
---|---|
NC_000001.11:g.220836629T>A , CM000663.2:g.220836629T>A | GRCh38 |
NC_000001.10:g.221009971T>A , CM000663.1:g.221009971T>A | GRCh37 |
NC_000001.9:g.219076594T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651706.1:c.842+31355T>A | ENSP00000499157.1:n.842+31355T>A | |
NR_046901.1:n.293-3437A>T |