HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45948021G>A , CM000682.2:g.45948021G>A | GRCh38 |
NC_000020.10:g.44576660G>A , CM000682.1:g.44576660G>A | GRCh37 |
NC_000020.9:g.44010067G>A | NCBI36 |
NG_029772.1:g.29174C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372409.7:c.*266G>A | ENSP00000361486.3:n.*266G>A | |
ENST00000479348.2:c.1322G>A | ||
NM_022104.3:c.*266G>A | NP_071387.1:n.*266G>A | |
XM_011528980.1:c.*266G>A | XP_011527282.1:n.*266G>A | |
XM_011528981.1:c.*266G>A | XP_011527283.1:n.*266G>A | |
XM_011528982.1:c.*266G>A | XP_011527284.1:n.*266G>A | |
XM_017028014.2:c.*266G>A | XP_016883503.1:n.*266G>A |