HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190414_204190415del , CM000663.2:g.204190414_204190415del | GRCh38 |
NC_000001.10:g.204159542_204159543del , CM000663.1:g.204159542_204159543del | GRCh37 |
NC_000001.9:g.202426165_202426166del | NCBI36 |
NG_032151.1:g.11078_11079del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*70_*71del MANE Select | ENSP00000356162.4:n.*70_*71del | |
ENST00000367194.4:c.*70_*71del | ENSP00000356162.4:n.*70_*71del | |
NM_002256.3:c.*70_*71del | NP_002247.3:n.*70_*71del | |
XM_011509525.1:c.*70_*71del | XP_011507827.1:n.*70_*71del | |
NM_002256.4:c.*70_*71del MANE Select | NP_002247.3:n.*70_*71del |