HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157114819T>A , CM000667.2:g.157114819T>A | GRCh38 |
NC_000005.9:g.156541830T>A , CM000667.1:g.156541830T>A | GRCh37 |
NC_000005.8:g.156474408T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-7857A>T | ENSP00000430328.2:n.-293-7857A>T | |
ENST00000524219.1:c.-293-7857A>T | ENSP00000430328.1:n.-293-7857A>T |