HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213656_1213657del , CM000667.2:g.1213656_1213657del | GRCh38 |
NC_000005.9:g.1213771_1213772del , CM000667.1:g.1213771_1213772del | GRCh37 |
NC_000005.8:g.1266771_1266772del | NCBI36 |
NG_008282.1:g.17062_17063del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.774+83_774+84del MANE Select | ENSP00000305302.10:n.774+83_774+84del | |
ENST00000304460.10:c.774+83_774+84del | ENSP00000305302.10:n.774+83_774+84del | |
ENST00000515652.5:c.682+83_682+84del | ENSP00000425701.1:n.682+83_682+84del | |
NM_001003841.2:c.774+83_774+84del | NP_001003841.1:n.774+83_774+84del | |
NM_001003841.3:c.774+83_774+84del MANE Select | NP_001003841.1:n.774+83_774+84del |