HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717287A>C , CM000674.2:g.12717287A>C | GRCh38 |
NC_000012.11:g.12870221A>C , CM000674.1:g.12870221A>C | GRCh37 |
NC_000012.10:g.12761488A>C | NCBI36 |
NG_016341.1:g.4920A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1538A>C (CDKN1B) | ||
ENST00000684771.1:n.585-1538A>C (CDKN1B) | ||
ENST00000228872.8:c.-553A>C (CDKN1B) | ENSP00000228872.4:n.-553A>C | |
ENST00000477087.1:n.154+1404A>C (CDKN1B) | ||
NM_004064.4:c.-553A>C (CDKN1B) | NP_004055.1:n.-553A>C | |
XM_011520623.3:c.-1781T>G (GPR19) | XP_011518925.1:n.-1781T>G | |
XM_017019216.2:c.-1809T>G (GPR19) | XP_016874705.1:n.-1809T>G |