HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135789816_135789817delinsAC , CM000664.2:g.135789816_135789817delinsAC | GRCh38 |
NC_000002.11:g.136547386_136547387delinsAC , CM000664.1:g.136547386_136547387delinsAC | GRCh37 |
NC_000002.10:g.136263856_136263857delinsAC | NCBI36 |
NG_008104.2:g.70353_70354delinsGT , LRG_338:g.70353_70354delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.5336-19_5336-18delinsGT MANE Select | ENSP00000264162.2:n.5336-19_5336-18delinsGT | |
ENST00000264162.6:c.5336-19_5336-18delinsGT | ENSP00000264162.2:n.5336-19_5336-18delinsGT | |
NM_002299.2:c.5336-19_5336-18delinsGT , LRG_338t1:c.5336-19_5336-18delinsGT | NP_002290.2:n.5336-19_5336-18delinsGT | |
NM_002299.3:c.5336-19_5336-18delinsGT | NP_002290.2:n.5336-19_5336-18delinsGT | |
NM_002299.4:c.5336-19_5336-18delinsGT MANE Select | NP_002290.2:n.5336-19_5336-18delinsGT |