HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717338T>C , CM000674.2:g.12717338T>C | GRCh38 |
NC_000012.11:g.12870272T>C , CM000674.1:g.12870272T>C | GRCh37 |
NC_000012.10:g.12761539T>C | NCBI36 |
NG_016341.1:g.4971T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1487T>C (CDKN1B) | ||
ENST00000684771.1:n.585-1487T>C (CDKN1B) | ||
ENST00000228872.8:c.-502T>C (CDKN1B) | ENSP00000228872.4:n.-502T>C | |
ENST00000477087.1:n.154+1455T>C (CDKN1B) | ||
NM_004064.4:c.-502T>C (CDKN1B) | NP_004055.1:n.-502T>C | |
XM_011520623.3:c.-1832A>G (GPR19) | XP_011518925.1:n.-1832A>G | |
XM_017019216.2:c.-1860A>G (GPR19) | XP_016874705.1:n.-1860A>G |