HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717325A>G , CM000674.2:g.12717325A>G | GRCh38 |
NC_000012.11:g.12870259A>G , CM000674.1:g.12870259A>G | GRCh37 |
NC_000012.10:g.12761526A>G | NCBI36 |
NG_016341.1:g.4958A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1500A>G (CDKN1B) | ||
ENST00000684771.1:n.585-1500A>G (CDKN1B) | ||
ENST00000228872.8:c.-515A>G (CDKN1B) | ENSP00000228872.4:n.-515A>G | |
ENST00000477087.1:n.154+1442A>G (CDKN1B) | ||
NM_004064.4:c.-515A>G (CDKN1B) | NP_004055.1:n.-515A>G | |
XM_011520623.3:c.-1819T>C (GPR19) | XP_011518925.1:n.-1819T>C | |
XM_017019216.2:c.-1847T>C (GPR19) | XP_016874705.1:n.-1847T>C |