HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717002C= , CM000674.2:g.12717002C= | GRCh38 |
NC_000012.11:g.12869936C= , CM000674.1:g.12869936C= | GRCh37 |
NC_000012.10:g.12761203C= | NCBI36 |
NG_016341.1:g.4635C= |
HGVS | Amino-acid Change |
---|---|
ENST00000477087.1:n.154+1119C= (CDKN1B) | |
ENST00000682620.1:n.1631-1823C= (CDKN1B) | |
ENST00000684771.1:n.585-1823C= (CDKN1B) | |
XM_011520623.1:c.-1496G= (GPR19) | XP_011518925.1:n.-1496G= |
XM_011520623.3:c.-1496G= (GPR19) | XP_011518925.1:n.-1496G= |
XM_017019216.2:c.-1524G= (GPR19) | XP_016874705.1:n.-1524G= |