HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65239975del , CM000674.2:g.65239975del | GRCh38 |
NC_000012.11:g.65633755del , CM000674.1:g.65633755del | GRCh37 |
NC_000012.10:g.63920022del | NCBI36 |
NG_016210.1:g.75405del | |
NG_016210.2:g.75405del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.1968del MANE Select | ENSP00000308369.2:p.Trp656Ter | |
ENST00000308330.2:c.1968del | ENSP00000308369.2:p.Trp656Ter | |
NM_001167614.1:c.1965del | NP_001161086.1:p.Trp655Ter | |
NM_014319.4:c.1968del | NP_055134.2:p.Trp656Ter | |
NM_014319.5:c.1968del MANE Select | NP_055134.2:p.Trp656Ter | |
NM_001167614.2:c.1965del | NP_001161086.1:p.Trp655Ter |