HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717279C>A , CM000674.2:g.12717279C>A | GRCh38 |
NC_000012.11:g.12870213C>A , CM000674.1:g.12870213C>A | GRCh37 |
NC_000012.10:g.12761480C>A | NCBI36 |
NG_016341.1:g.4912C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1546C>A (CDKN1B) | ||
ENST00000684771.1:n.585-1546C>A (CDKN1B) | ||
ENST00000228872.8:c.-561C>A (CDKN1B) | ENSP00000228872.4:n.-561C>A | |
ENST00000477087.1:n.154+1396C>A (CDKN1B) | ||
NM_004064.4:c.-561C>A (CDKN1B) | NP_004055.1:n.-561C>A | |
XM_011520623.3:c.-1773G>T (GPR19) | XP_011518925.1:n.-1773G>T | |
XM_017019216.2:c.-1801G>T (GPR19) | XP_016874705.1:n.-1801G>T |