HGVS | Genome Assembly |
---|---|
NC_000011.10:g.68685525_68685543del , CM000673.2:g.68685525_68685543del | GRCh38 |
NC_000011.9:g.68452993_68453011del , CM000673.1:g.68452993_68453011del | GRCh37 |
NC_000011.8:g.68209569_68209587del | NCBI36 |
NG_052785.1:g.6051_6069del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265643.4:c.82-69_82-51del MANE Select | ENSP00000265643.3:n.82-69_82-51del | |
ENST00000265643.3:c.82-69_82-51del | ENSP00000265643.3:n.82-69_82-51del | |
NM_015973.3:c.82-69_82-51del | NP_057057.2:n.82-69_82-51del | |
NM_015973.4:c.82-69_82-51del | NP_057057.2:n.82-69_82-51del | |
XR_001748281.1:n.230+2301_230+2319del | ||
NM_015973.5:c.82-69_82-51del MANE Select | NP_057057.2:n.82-69_82-51del |