HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8015733_8015735delinsATC , CM000679.2:g.8015733_8015735delinsATC | GRCh38 |
NC_000017.10:g.7919051_7919053delinsATC , CM000679.1:g.7919051_7919053delinsATC | GRCh37 |
NC_000017.9:g.7859776_7859778delinsATC | NCBI36 |
NG_009092.1:g.18064_18066delinsATC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.2945-10_2945-8delinsATC MANE Select | ENSP00000254854.4:n.2945-10_2945-8delinsATC | |
ENST00000254854.4:c.2945-10_2945-8delinsATC | ENSP00000254854.4:n.2945-10_2945-8delinsATC | |
NM_000180.3:c.2945-10_2945-8delinsATC | NP_000171.1:n.2945-10_2945-8delinsATC | |
XM_011523816.1:c.2945-10_2945-8delinsATC | XP_011522118.1:n.2945-10_2945-8delinsATC | |
NM_000180.4:c.2945-10_2945-8delinsATC MANE Select | NP_000171.1:n.2945-10_2945-8delinsATC |