HGVS | Genome Assembly |
---|---|
NC_000011.10:g.14893695C>T , CM000673.2:g.14893695C>T | GRCh38 |
NC_000011.9:g.14915241C>T , CM000673.1:g.14915241C>T | GRCh37 |
NC_000011.8:g.14871817C>T | NCBI36 |
NG_007936.1:g.3511G>A |
HGVS | Amino-acid change | |
---|---|---|
XM_011519898.1:c.-1451G>A | XP_011518200.1:n.-1451G>A | |
XM_011519898.3:c.-1451G>A | XP_011518200.1:n.-1451G>A |