HGVS | Genome Assembly |
---|---|
NC_000023.11:g.30304473del , CM000685.2:g.30304473del | GRCh38 |
NC_000023.10:g.30322590del , CM000685.1:g.30322590del | GRCh37 |
NC_000023.9:g.30232511del | NCBI36 |
NG_009814.1:g.9910del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378970.5:c.*110del MANE Select | ENSP00000368253.4:n.*110del | |
ENST00000378970.4:c.*110del | ENSP00000368253.4:n.*110del | |
NM_000475.4:c.*110del | NP_000466.2:n.*110del | |
NM_000475.5:c.*110del MANE Select | NP_000466.2:n.*110del |