HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95324225_95324227del , CM000669.2:g.95324225_95324227del | GRCh38 |
NC_000007.13:g.94953537_94953539del , CM000669.1:g.94953537_94953539del | GRCh37 |
NC_000007.12:g.94791473_94791475del | NCBI36 |
NG_008779.1:g.5348_5350del | |
NG_008779.2:g.5482_5484del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.74+177_74+179del MANE Select | ENSP00000222381.3:n.74+177_74+179del | |
ENST00000222381.7:c.74+177_74+179del | ENSP00000222381.3:n.74+177_74+179del | |
ENST00000433729.1:c.74+177_74+179del | ENSP00000407359.1:n.74+177_74+179del | |
NM_000446.5:c.74+177_74+179del | NP_000437.3:n.74+177_74+179del | |
NM_000446.6:c.74+177_74+179del | NP_000437.3:n.74+177_74+179del | |
NM_000446.7:c.74+177_74+179del MANE Select | NP_000437.3:n.74+177_74+179del |