HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717313C>T , CM000674.2:g.12717313C>T | GRCh38 |
NC_000012.11:g.12870247C>T , CM000674.1:g.12870247C>T | GRCh37 |
NC_000012.10:g.12761514C>T | NCBI36 |
NG_016341.1:g.4946C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1512C>T (CDKN1B) | ||
ENST00000684771.1:n.585-1512C>T (CDKN1B) | ||
ENST00000228872.8:c.-527C>T (CDKN1B) | ENSP00000228872.4:n.-527C>T | |
ENST00000477087.1:n.154+1430C>T (CDKN1B) | ||
NM_004064.4:c.-527C>T (CDKN1B) | NP_004055.1:n.-527C>T | |
XM_011520623.3:c.-1807G>A (GPR19) | XP_011518925.1:n.-1807G>A | |
XM_017019216.2:c.-1835G>A (GPR19) | XP_016874705.1:n.-1835G>A |