HGVS | Genome Assembly |
---|---|
NC_000014.9:g.99609502G>A , CM000676.2:g.99609502G>A | GRCh38 |
NC_000014.8:g.100075839G>A , CM000676.1:g.100075839G>A | GRCh37 |
NC_000014.7:g.99145592G>A | NCBI36 |
NG_051108.1:g.10027G>A |
HGVS | Amino-acid change | |
---|---|---|
XM_006720277.2:c.-199+4887G>A | XP_006720340.1:n.-199+4887G>A | |
XM_011537236.1:c.-287+4887G>A | XP_011535538.1:n.-287+4887G>A | |
NM_001329411.1:c.-287+4887G>A | NP_001316340.1:n.-287+4887G>A | |
XM_006720277.3:c.-199+4887G>A | XP_006720340.1:n.-199+4887G>A | |
XM_011537236.2:c.-287+4887G>A | XP_011535538.1:n.-287+4887G>A | |
NM_001329411.2:c.-287+4887G>A | NP_001316340.1:n.-287+4887G>A |