HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869122_240869129del , CM000664.2:g.240869122_240869129del | GRCh38 |
NC_000002.11:g.241808539_241808546del , CM000664.1:g.241808539_241808546del | GRCh37 |
NC_000002.10:g.241457212_241457219del | NCBI36 |
NG_008005.1:g.5378_5385del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.166-48_166-41del MANE Select | ENSP00000302620.3:n.166-48_166-41del | |
ENST00000307503.3:c.166-48_166-41del | ENSP00000302620.3:n.166-48_166-41del | |
ENST00000472436.1:n.186-48_186-41del | ||
NM_000030.2:c.166-48_166-41del | NP_000021.1:n.166-48_166-41del | |
XR_924060.1:n.405+1104_405+1111del | ||
NM_000030.3:c.166-48_166-41del MANE Select | NP_000021.1:n.166-48_166-41del |