HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190412_204190413del , CM000663.2:g.204190412_204190413del | GRCh38 |
NC_000001.10:g.204159540_204159541del , CM000663.1:g.204159540_204159541del | GRCh37 |
NC_000001.9:g.202426163_202426164del | NCBI36 |
NG_032151.1:g.11081_11082del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*73_*74del MANE Select | ENSP00000356162.4:n.*73_*74del | |
ENST00000367194.4:c.*73_*74del | ENSP00000356162.4:n.*73_*74del | |
NM_002256.3:c.*73_*74del | NP_002247.3:n.*73_*74del | |
XM_011509525.1:c.*73_*74del | XP_011507827.1:n.*73_*74del | |
NM_002256.4:c.*73_*74del MANE Select | NP_002247.3:n.*73_*74del |