HGVS | Genome Assembly |
---|---|
NC_000001.11:g.10972963_10972964dup , CM000663.2:g.10972963_10972964dup | GRCh38 |
NC_000001.10:g.11033020_11033021dup , CM000663.1:g.11033020_11033021dup | GRCh37 |
NC_000001.9:g.10955607_10955608dup | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377004.9:c.128-2866_128-2865dup MANE Select | ENSP00000366203.4:n.128-2866_128-2865dup | |
ENST00000377004.8:c.128-2866_128-2865dup | ENSP00000366203.4:n.128-2866_128-2865dup | |
ENST00000520253.1:c.61-2866_61-2865dup | ||
NM_001170754.1:c.128-2866_128-2865dup | NP_001164225.1:n.128-2866_128-2865dup | |
NM_001170754.2:c.128-2866_128-2865dup MANE Select | NP_001164225.1:n.128-2866_128-2865dup |