HGVS | Genome Assembly |
---|---|
NC_000019.10:g.853419del , CM000681.2:g.853419del | GRCh38 |
NC_000019.9:g.853419del , CM000681.1:g.853419del | GRCh37 |
NC_000019.8:g.804419del | NCBI36 |
NG_009627.1:g.6129del , LRG_57:g.6129del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263621.2:c.366+16del MANE Select | ENSP00000263621.1:n.366+16del | |
ENST00000263621.1:c.366+16del | ENSP00000263621.1:n.366+16del | |
ENST00000590230.5:c.366+16del | ENSP00000466090.1:n.366+16del | |
NM_001972.2:c.366+16del , LRG_57t1:c.366+16del | NP_001963.1:n.366+16del | |
XM_011527775.1:c.366+16del | XP_011526077.1:n.366+16del | |
XM_011527776.1:c.366+16del | XP_011526078.1:n.366+16del | |
NM_001972.3:c.366+16del | NP_001963.1:n.366+16del | |
NM_001972.4:c.366+16del MANE Select | NP_001963.1:n.366+16del |