HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135790043_135790044delinsCG , CM000664.2:g.135790043_135790044delinsCG | GRCh38 |
NC_000002.11:g.136547613_136547614delinsCG , CM000664.1:g.136547613_136547614delinsCG | GRCh37 |
NC_000002.10:g.136264083_136264084delinsCG | NCBI36 |
NG_008104.2:g.70126_70127delinsCG , LRG_338:g.70126_70127delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.5336-246_5336-245delinsCG MANE Select | ENSP00000264162.2:n.5336-246_5336-245delinsCG | |
ENST00000264162.6:c.5336-246_5336-245delinsCG | ENSP00000264162.2:n.5336-246_5336-245delinsCG | |
NM_002299.2:c.5336-246_5336-245delinsCG , LRG_338t1:c.5336-246_5336-245delinsCG | NP_002290.2:n.5336-246_5336-245delinsCG | |
NM_002299.3:c.5336-246_5336-245delinsCG | NP_002290.2:n.5336-246_5336-245delinsCG | |
NM_002299.4:c.5336-246_5336-245delinsCG MANE Select | NP_002290.2:n.5336-246_5336-245delinsCG |