HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717269C>T , CM000674.2:g.12717269C>T | GRCh38 |
NC_000012.11:g.12870203C>T , CM000674.1:g.12870203C>T | GRCh37 |
NC_000012.10:g.12761470C>T | NCBI36 |
NG_016341.1:g.4902C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1556C>T (CDKN1B) | ||
ENST00000684771.1:n.585-1556C>T (CDKN1B) | ||
ENST00000228872.8:c.-571C>T (CDKN1B) | ENSP00000228872.4:n.-571C>T | |
ENST00000477087.1:n.154+1386C>T (CDKN1B) | ||
XM_011520623.1:c.-1763G>A (GPR19) | XP_011518925.1:n.-1763G>A | |
XM_011520623.3:c.-1763G>A (GPR19) | XP_011518925.1:n.-1763G>A | |
XM_017019216.2:c.-1791G>A (GPR19) | XP_016874705.1:n.-1791G>A |