HGVS | Genome Assembly |
---|---|
NC_000014.9:g.99609387A= , CM000676.2:g.99609387A= | GRCh38 |
NC_000014.8:g.100075724A= , CM000676.1:g.100075724A= | GRCh37 |
NC_000014.7:g.99145477A= | NCBI36 |
NG_051108.1:g.9912A= |
HGVS | Amino-acid Change | |
---|---|---|
XM_006720277.2:c.-199+4772A= | XP_006720340.1:n.-199+4772A= | |
XM_011537236.1:c.-287+4772A= | XP_011535538.1:n.-287+4772A= | |
NM_001329411.1:c.-287+4772A= | NP_001316340.1:n.-287+4772A= | |
XM_006720277.3:c.-199+4772A= | XP_006720340.1:n.-199+4772A= | |
XM_011537236.2:c.-287+4772A= | XP_011535538.1:n.-287+4772A= | |
NM_001329411.2:c.-287+4772A= | NP_001316340.1:n.-287+4772A= |