HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717299G>T , CM000674.2:g.12717299G>T | GRCh38 |
NC_000012.11:g.12870233G>T , CM000674.1:g.12870233G>T | GRCh37 |
NC_000012.10:g.12761500G>T | NCBI36 |
NG_016341.1:g.4932G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1526G>T (CDKN1B) | ||
ENST00000684771.1:n.585-1526G>T (CDKN1B) | ||
ENST00000228872.8:c.-541G>T (CDKN1B) | ENSP00000228872.4:n.-541G>T | |
ENST00000477087.1:n.154+1416G>T (CDKN1B) | ||
NM_004064.4:c.-541G>T (CDKN1B) | NP_004055.1:n.-541G>T | |
XM_011520623.3:c.-1793C>A (GPR19) | XP_011518925.1:n.-1793C>A | |
XM_017019216.2:c.-1821C>A (GPR19) | XP_016874705.1:n.-1821C>A |