HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12715152G>A , CM000674.2:g.12715152G>A | GRCh38 |
NC_000012.11:g.12868086G>A , CM000674.1:g.12868086G>A | GRCh37 |
NC_000012.10:g.12759353G>A | NCBI36 |
NG_016341.1:g.2785G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682080.1:n.2305G>A (CDKN1B) | ||
ENST00000682620.1:n.1631-3673G>A (CDKN1B) | ||
ENST00000684771.1:n.585-3673G>A (CDKN1B) | ||
ENST00000477087.1:n.47+48G>A (CDKN1B) | ||
XM_011520623.1:c.-205+559C>T (GPR19) | XP_011518925.1:n.-205+559C>T | |
XM_011520623.3:c.-205+559C>T (GPR19) | XP_011518925.1:n.-205+559C>T | |
XM_017019216.2:c.-233+559C>T (GPR19) | XP_016874705.1:n.-233+559C>T |