HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717316A>G , CM000674.2:g.12717316A>G | GRCh38 |
NC_000012.11:g.12870250A>G , CM000674.1:g.12870250A>G | GRCh37 |
NC_000012.10:g.12761517A>G | NCBI36 |
NG_016341.1:g.4949A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1509A>G (CDKN1B) | ||
ENST00000684771.1:n.585-1509A>G (CDKN1B) | ||
ENST00000228872.8:c.-524A>G (CDKN1B) | ENSP00000228872.4:n.-524A>G | |
ENST00000477087.1:n.154+1433A>G (CDKN1B) | ||
NM_004064.4:c.-524A>G (CDKN1B) | NP_004055.1:n.-524A>G | |
XM_011520623.3:c.-1810T>C (GPR19) | XP_011518925.1:n.-1810T>C | |
XM_017019216.2:c.-1838T>C (GPR19) | XP_016874705.1:n.-1838T>C |