HGVS | Genome Assembly |
---|---|
NC_000014.9:g.52322424_52322425del , CM000676.2:g.52322424_52322425del | GRCh38 |
NC_000014.8:g.52789142_52789143del , CM000676.1:g.52789142_52789143del | GRCh37 |
NC_000014.7:g.51858892_51858893del | NCBI36 |
NG_013082.1:g.13127_13128del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245457.6:c.844-4797_844-4796del MANE Select | ENSP00000245457.5:n.844-4797_844-4796del | |
ENST00000245457.5:c.844-4797_844-4796del | ENSP00000245457.5:n.844-4797_844-4796del | |
ENST00000557436.1:c.79-4797_79-4796del | ENSP00000450933.1:n.79-4797_79-4796del | |
NM_000956.3:c.844-4797_844-4796del | NP_000947.2:n.844-4797_844-4796del | |
NM_000956.4:c.844-4797_844-4796del MANE Select | NP_000947.2:n.844-4797_844-4796del |