HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21129476A>G , CM000674.2:g.21129476A>G | GRCh38 |
NC_000012.11:g.21282410A>G , CM000674.1:g.21282410A>G | GRCh37 |
NC_000012.10:g.21173677A>G | NCBI36 |
NG_011745.1:g.3283A>G , LRG_1022:g.3283A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000543498.5:c.281-12038A>G | ||
ENST00000585342.5:c.371-1647A>G | ENSP00000467594.1:n.371-1647A>G | |
ENST00000590779.5:c.377-1647A>G | ||
ENST00000592513.1:c.358-1647A>G | ||
ENST00000593147.5:c.406-1647A>G | ENSP00000467209.1:n.406-1647A>G |