HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81649192dup , CM000665.2:g.81649192dup | GRCh38 |
NC_000003.11:g.81698343dup , CM000665.1:g.81698343dup | GRCh37 |
NC_000003.10:g.81781033dup | NCBI36 |
NG_011810.1:g.117609dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.556-201dup MANE Select | ENSP00000410833.2:n.556-201dup | |
ENST00000429644.6:c.556-201dup | ENSP00000410833.2:n.556-201dup | |
ENST00000486920.1:n.552-201dup | ||
ENST00000489715.1:c.433-201dup | ENSP00000419638.1:n.433-201dup | |
ENST00000498468.1:n.84-201dup | ||
NM_000158.3:c.556-201dup | NP_000149.3:n.556-201dup | |
NM_000158.4:c.556-201dup MANE Select | NP_000149.4:n.556-201dup |