HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188991612_188991633dup , CM000664.2:g.188991612_188991633dup | GRCh38 |
NC_000002.11:g.189856338_189856359dup , CM000664.1:g.189856338_189856359dup | GRCh37 |
NC_000002.10:g.189564583_189564604dup | NCBI36 |
NG_007404.1:g.22240_22261dup , LRG_3:g.22240_22261dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.898-57_898-36dup | ENSP00000415346.2:n.898-57_898-36dup | |
ENST00000304636.9:c.898-57_898-36dup MANE Select | ENSP00000304408.4:n.898-57_898-36dup | |
ENST00000304636.7:c.898-57_898-36dup | ENSP00000304408.3:n.898-57_898-36dup | |
ENST00000317840.9:c.898-57_898-36dup | ENSP00000315243.6:n.898-57_898-36dup | |
NM_000090.3:c.898-57_898-36dup , LRG_3t1:c.898-57_898-36dup | NP_000081.1:n.898-57_898-36dup | |
NM_000090.4:c.898-57_898-36dup MANE Select | NP_000081.2:n.898-57_898-36dup |