HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135817202del , CM000664.2:g.135817202del | GRCh38 |
NC_000002.11:g.136574772del , CM000664.1:g.136574772del | GRCh37 |
NC_000002.10:g.136291242del | NCBI36 |
NG_008104.2:g.42969del , LRG_338:g.42969del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.1707+140del MANE Select | ENSP00000264162.2:n.1707+140del | |
ENST00000264162.6:c.1707+140del | ENSP00000264162.2:n.1707+140del | |
NM_002299.2:c.1707+140del , LRG_338t1:c.1707+140del | NP_002290.2:n.1707+140del | |
NM_002299.3:c.1707+140del | NP_002290.2:n.1707+140del | |
XM_017004088.2:c.1707+140del | XP_016859577.1:n.1707+140del | |
NM_002299.4:c.1707+140del MANE Select | NP_002290.2:n.1707+140del |