HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107767764dup , CM000669.2:g.107767764dup | GRCh38 |
NC_000007.13:g.107408209dup , CM000669.1:g.107408209dup | GRCh37 |
NC_000007.12:g.107195445dup | NCBI36 |
NG_008046.1:g.40470dup , LRG_683:g.40470dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000340010.10:c.2205+2dup MANE Select | ENSP00000345873.5:n.2205+2dup | |
ENST00000340010.9:c.2205+2dup | ENSP00000345873.5:n.2205+2dup | |
ENST00000379083.7:c.*1762+2dup | ENSP00000368375.3:n.*1762+2dup | |
NM_000111.2:c.2205+2dup , LRG_683t1:c.2205+2dup | NP_000102.1:n.2205+2dup | |
XM_011515867.1:c.2205+2dup | XP_011514169.1:n.2205+2dup | |
NM_000111.3:c.2205+2dup MANE Select | NP_000102.1:n.2205+2dup |