HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717270_12717273dup , CM000674.2:g.12717270_12717273dup | GRCh38 |
NC_000012.11:g.12870204_12870207dup , CM000674.1:g.12870204_12870207dup | GRCh37 |
NC_000012.10:g.12761471_12761474dup | NCBI36 |
NG_016341.1:g.4903_4906dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1555_1631-1552dup (CDKN1B) | ||
ENST00000684771.1:n.585-1555_585-1552dup (CDKN1B) | ||
ENST00000228872.8:c.-570_-567dup (CDKN1B) | ENSP00000228872.4:n.-570_-567dup | |
ENST00000477087.1:n.154+1387_154+1390dup (CDKN1B) | ||
NM_004064.4:c.-570_-567dup (CDKN1B) | NP_004055.1:n.-570_-567dup | |
XM_011520623.3:c.-1767_-1764dup (GPR19) | XP_011518925.1:n.-1767_-1764dup | |
XM_017019216.2:c.-1795_-1792dup (GPR19) | XP_016874705.1:n.-1795_-1792dup |