HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63962098_63962100del , CM000667.2:g.63962098_63962100del | GRCh38 |
NC_000005.9:g.63257925_63257927del , CM000667.1:g.63257925_63257927del | GRCh37 |
NC_000005.8:g.63293681_63293683del | NCBI36 |
NG_032816.1:g.5193_5195del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000323865.5:c.-381_-379del MANE Select | ENSP00000316244.4:n.-381_-379del | |
ENST00000323865.4:c.-381_-379del | ENSP00000316244.3:n.-381_-379del | |
ENST00000506598.1:c.-381_-379del | ENSP00000423433.1:n.-381_-379del | |
NM_000524.3:c.-381_-379del | NP_000515.2:n.-381_-379del | |
NM_000524.4:c.-381_-379del MANE Select | NP_000515.2:n.-381_-379del |