HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135817040dup , CM000664.2:g.135817040dup | GRCh38 |
NC_000002.11:g.136574610dup , CM000664.1:g.136574610dup | GRCh37 |
NC_000002.10:g.136291080dup | NCBI36 |
NG_008104.2:g.43134dup , LRG_338:g.43134dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.1707+305dup MANE Select | ENSP00000264162.2:n.1707+305dup | |
ENST00000264162.6:c.1707+305dup | ENSP00000264162.2:n.1707+305dup | |
NM_002299.2:c.1707+305dup , LRG_338t1:c.1707+305dup | NP_002290.2:n.1707+305dup | |
NM_002299.3:c.1707+305dup | NP_002290.2:n.1707+305dup | |
XM_017004088.2:c.1707+305dup | XP_016859577.1:n.1707+305dup | |
NM_002299.4:c.1707+305dup MANE Select | NP_002290.2:n.1707+305dup |