HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63962117_63962118dup , CM000667.2:g.63962117_63962118dup | GRCh38 |
NC_000005.9:g.63257944_63257945dup , CM000667.1:g.63257944_63257945dup | GRCh37 |
NC_000005.8:g.63293700_63293701dup | NCBI36 |
NG_032816.1:g.5177_5178dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000323865.5:c.-397_-396dup MANE Select | ENSP00000316244.4:n.-397_-396dup | |
ENST00000323865.4:c.-397_-396dup | ENSP00000316244.3:n.-397_-396dup | |
ENST00000506598.1:c.-387-10_-387-9dup | ENSP00000423433.1:n.-387-10_-387-9dup | |
NM_000524.3:c.-397_-396dup | NP_000515.2:n.-397_-396dup | |
NM_000524.4:c.-397_-396dup MANE Select | NP_000515.2:n.-397_-396dup |