HGVS | Genome Assembly |
---|---|
NC_000017.11:g.35880685G>A , CM000679.2:g.35880685G>A | GRCh38 |
NC_000017.9:g.31231802G>A | NCBI36 |
NG_015990.1:g.4689C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000605509.2:c.-18+44C>T | ENSP00000474141.2:n.-18+44C>T | |
ENST00000605140.5:c.-18+44C>T | ENSP00000475057.1:n.-18+44C>T | |
XR_934696.1:n.197-3697G>A | ||
XR_934697.1:n.200-3697G>A | ||
XR_001752852.1:n.426+611G>A | ||
XR_934696.2:n.91-3697G>A | ||
XR_934697.2:n.91-3697G>A |