HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215782038_215782041dup , CM000663.2:g.215782038_215782041dup | GRCh38 |
NC_000001.10:g.215955380_215955383dup , CM000663.1:g.215955380_215955383dup | GRCh37 |
NC_000001.9:g.214022003_214022006dup | NCBI36 |
NG_009497.1:g.646357_646360dup | |
NG_009497.2:g.646409_646412dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.10740+2_10740+5dup MANE Select | ENSP00000305941.3:n.10740+2_10740+5dup | |
ENST00000674083.1:c.10740+2_10740+5dup | ENSP00000501296.1:n.10740+2_10740+5dup | |
ENST00000307340.7:c.10740+2_10740+5dup | ENSP00000305941.3:n.10740+2_10740+5dup | |
NM_206933.2:c.10740+2_10740+5dup | NP_996816.2:n.10740+2_10740+5dup | |
NM_206933.3:c.10740+2_10740+5dup | NP_996816.2:n.10740+2_10740+5dup | |
NM_206933.4:c.10740+2_10740+5dup MANE Select | NP_996816.3:n.10740+2_10740+5dup |