HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67940851_67940855dup , CM000678.2:g.67940851_67940855dup | GRCh38 |
NC_000016.9:g.67974754_67974758dup , CM000678.1:g.67974754_67974758dup | GRCh37 |
NC_000016.8:g.66532255_66532259dup | NCBI36 |
NG_009778.1:g.8273_8277dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.749-362_749-358dup MANE Select | ENSP00000264005.5:n.749-362_749-358dup | |
ENST00000264005.9:c.749-362_749-358dup | ENSP00000264005.5:n.749-362_749-358dup | |
ENST00000570369.5:c.156-766_156-762dup | ||
ENST00000570980.1:c.533-362_533-358dup | ENSP00000464651.1:n.533-362_533-358dup | |
ENST00000573538.5:c.392-9_392-5dup | ENSP00000463220.1:n.392-9_392-5dup | |
NM_000229.1:c.749-362_749-358dup | NP_000220.1:n.749-362_749-358dup | |
NM_000229.2:c.749-362_749-358dup MANE Select | NP_000220.1:n.749-362_749-358dup |