HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73640875dup , CM000664.2:g.73640875dup | GRCh38 |
NC_000002.11:g.73868002dup , CM000664.1:g.73868002dup | GRCh37 |
NC_000002.10:g.73721510dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.*70dup MANE Select | ENSP00000272425.3:n.*70dup | |
ENST00000272425.3:c.*70dup | ENSP00000272425.3:n.*70dup | |
NM_003960.3:c.*70dup | NP_003951.3:n.*70dup | |
NM_003960.4:c.*70dup MANE Select | NP_003951.3:n.*70dup |