HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154905052_154905053del , CM000685.2:g.154905052_154905053del | GRCh38 |
NC_000023.10:g.154133327_154133328del , CM000685.1:g.154133327_154133328del | GRCh37 |
NC_000023.9:g.153786521_153786522del | NCBI36 |
NG_011403.1:g.122681_122682del | |
NG_011403.2:g.122681_122682del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5374-20_5374-19del MANE Select | ENSP00000353393.4:n.5374-20_5374-19del | |
ENST00000360256.8:c.5374-20_5374-19del | ENSP00000353393.4:n.5374-20_5374-19del | |
NM_000132.3:c.5374-20_5374-19del | NP_000123.1:n.5374-20_5374-19del | |
XM_011531126.1:c.5269-20_5269-19del | XP_011529428.1:n.5269-20_5269-19del | |
NM_000132.4:c.5374-20_5374-19del MANE Select | NP_000123.1:n.5374-20_5374-19del |