HGVS | Genome Assembly |
---|---|
NC_000007.14:g.20164420del , CM000669.2:g.20164420del | GRCh38 |
NC_000007.13:g.20204043del , CM000669.1:g.20204043del | GRCh37 |
NC_000007.12:g.20170568del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000400331.10:c.-152-16del MANE Select | ENSP00000383185.3:n.-152-16del | |
ENST00000332878.8:c.-8-2545del | ENSP00000328410.4:n.-8-2545del | |
ENST00000400331.9:c.-152-16del | ENSP00000383185.3:n.-152-16del | |
ENST00000471019.1:n.274-16del | ||
ENST00000589011.1:c.-8-2545del | ENSP00000466864.1:n.-8-2545del | |
NM_182762.3:c.-152-16del | NP_877439.3:n.-152-16del | |
NM_182762.4:c.-152-16del MANE Select | NP_877439.3:n.-152-16del |