HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135833097dup , CM000664.2:g.135833097dup | GRCh38 |
NC_000002.11:g.136590667dup , CM000664.1:g.136590667dup | GRCh37 |
NC_000002.10:g.136307137dup | NCBI36 |
NG_008104.2:g.27077dup , LRG_338:g.27077dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.720+18dup MANE Select | ENSP00000264162.2:n.720+18dup | |
ENST00000264162.6:c.720+18dup | ENSP00000264162.2:n.720+18dup | |
NM_002299.2:c.720+18dup , LRG_338t1:c.720+18dup | NP_002290.2:n.720+18dup | |
NM_002299.3:c.720+18dup | NP_002290.2:n.720+18dup | |
XM_017004088.2:c.720+18dup | XP_016859577.1:n.720+18dup | |
NM_002299.4:c.720+18dup MANE Select | NP_002290.2:n.720+18dup |