HGVS | Genome Assembly |
---|---|
NC_000020.11:g.62473307_62473313del , CM000682.2:g.62473307_62473313del | GRCh38 |
NC_000020.10:g.61048363_61048369del , CM000682.1:g.61048363_61048369del | GRCh37 |
NC_000020.9:g.60481758_60481764del | NCBI36 |
NG_046963.1:g.7667_7673del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252997.3:c.699+99_699+105del MANE Select | ENSP00000252997.2:n.699+99_699+105del | |
ENST00000252997.2:c.699+99_699+105del | ENSP00000252997.2:n.699+99_699+105del | |
NM_080473.4:c.699+99_699+105del | NP_536721.1:n.699+99_699+105del | |
XM_006723699.2:c.699+99_699+105del | XP_006723762.1:n.699+99_699+105del | |
XM_006723699.3:c.699+99_699+105del | XP_006723762.1:n.699+99_699+105del | |
NM_080473.5:c.699+99_699+105del MANE Select | NP_536721.1:n.699+99_699+105del |