HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717321A= , CM000674.2:g.12717321A= | GRCh38 |
NC_000012.11:g.12870255A= , CM000674.1:g.12870255A= | GRCh37 |
NC_000012.10:g.12761522A= | NCBI36 |
NG_016341.1:g.4954A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1504A= (CDKN1B) | ||
ENST00000684771.1:n.585-1504A= (CDKN1B) | ||
ENST00000228872.8:c.-519A= (CDKN1B) | ENSP00000228872.4:n.-519A= | |
ENST00000477087.1:n.154+1438A= (CDKN1B) | ||
NM_004064.4:c.-519A= (CDKN1B) | NP_004055.1:n.-519A= | |
XM_011520623.3:c.-1815T= (GPR19) | XP_011518925.1:n.-1815T= | |
XM_017019216.2:c.-1843T= (GPR19) | XP_016874705.1:n.-1843T= |