HGVS | Genome Assembly |
---|---|
NC_000020.11:g.4234938_4234939delinsGT , CM000682.2:g.4234938_4234939delinsGT | GRCh38 |
NC_000020.10:g.4215585_4215586delinsGT , CM000682.1:g.4215585_4215586delinsGT | GRCh37 |
NC_000020.9:g.4163585_4163586delinsGT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379453.6:c.1112-12809_1112-12808delinsAC MANE Select | ENSP00000368766.4:n.1112-12809_1112-12808... | |
ENST00000379453.5:c.1112-12809_1112-12808delinsAC | ENSP00000368766.4:n.1112-12809_1112-12808... | |
NM_000678.3:c.1112-12809_1112-12808delinsAC | NP_000669.1:n.1112-12809_1112-12808delins... | |
NM_000678.4:c.1112-12809_1112-12808delinsAC MANE Select | NP_000669.1:n.1112-12809_1112-12808delins... |