HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135790046_135790047delinsGA , CM000664.2:g.135790046_135790047delinsGA | GRCh38 |
NC_000002.11:g.136547616_136547617delinsGA , CM000664.1:g.136547616_136547617delinsGA | GRCh37 |
NC_000002.10:g.136264086_136264087delinsGA | NCBI36 |
NG_008104.2:g.70123_70124delinsTC , LRG_338:g.70123_70124delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.5336-249_5336-248delinsTC MANE Select | ENSP00000264162.2:n.5336-249_5336-248delinsTC | |
ENST00000264162.6:c.5336-249_5336-248delinsTC | ENSP00000264162.2:n.5336-249_5336-248delinsTC | |
NM_002299.2:c.5336-249_5336-248delinsTC , LRG_338t1:c.5336-249_5336-248delinsTC | NP_002290.2:n.5336-249_5336-248delinsTC | |
NM_002299.3:c.5336-249_5336-248delinsTC | NP_002290.2:n.5336-249_5336-248delinsTC | |
NM_002299.4:c.5336-249_5336-248delinsTC MANE Select | NP_002290.2:n.5336-249_5336-248delinsTC |