HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717258_12717259dup , CM000674.2:g.12717258_12717259dup | GRCh38 |
NC_000012.11:g.12870192_12870193dup , CM000674.1:g.12870192_12870193dup | GRCh37 |
NC_000012.10:g.12761459_12761460dup | NCBI36 |
NG_016341.1:g.4891_4892dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1567_1631-1566dup (CDKN1B) | ||
ENST00000684771.1:n.585-1567_585-1566dup (CDKN1B) | ||
ENST00000228872.8:c.-582_-581dup (CDKN1B) | ENSP00000228872.4:n.-582_-581dup | |
ENST00000477087.1:n.154+1375_154+1376dup (CDKN1B) | ||
XM_011520623.1:c.-1750_-1749dup (GPR19) | XP_011518925.1:n.-1750_-1749dup | |
XM_011520623.3:c.-1750_-1749dup (GPR19) | XP_011518925.1:n.-1750_-1749dup | |
XM_017019216.2:c.-1778_-1777dup (GPR19) | XP_016874705.1:n.-1778_-1777dup |