HGVS | Genome Assembly |
---|---|
NC_000014.9:g.99609588G= , CM000676.2:g.99609588G= | GRCh38 |
NC_000014.8:g.100075925G= , CM000676.1:g.100075925G= | GRCh37 |
NC_000014.7:g.99145678G= | NCBI36 |
NG_051108.1:g.10113G= |
HGVS | Amino-acid Change | |
---|---|---|
XM_006720277.2:c.-199+4973G= | XP_006720340.1:n.-199+4973G= | |
XM_011537236.1:c.-287+4973G= | XP_011535538.1:n.-287+4973G= | |
NM_001329411.1:c.-287+4973G= | NP_001316340.1:n.-287+4973G= | |
XM_006720277.3:c.-199+4973G= | XP_006720340.1:n.-199+4973G= | |
XM_011537236.2:c.-287+4973G= | XP_011535538.1:n.-287+4973G= | |
NM_001329411.2:c.-287+4973G= | NP_001316340.1:n.-287+4973G= |