HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85589284_85589297delinsTGTGTATATAGTCA , CM000664.2:g.85589284_85589297delinsTGTGTATATAGTCA | GRCh38 |
NC_000002.11:g.85816407_85816420delinsTGTGTATATAGTCA , CM000664.1:g.85816407_85816420delinsTGTGTATATAGTCA | GRCh37 |
NC_000002.10:g.85669918_85669931delinsTGTGTATATAGTCA | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306384.5:c.4-2441_4-2428delinsTGTGTATATAGTCA MANE Select | ENSP00000305647.4:n.4-2441_4-2428delinsTG... | |
ENST00000306384.4:c.4-2441_4-2428delinsTGTGTATATAGTCA | ENSP00000305647.4:n.4-2441_4-2428delinsTG... | |
NM_006634.2:c.4-2441_4-2428delinsTGTGTATATAGTCA | NP_006625.1:n.4-2441_4-2428delinsTGTGTATA... | |
NM_006634.3:c.4-2441_4-2428delinsTGTGTATATAGTCA MANE Select | NP_006625.1:n.4-2441_4-2428delinsTGTGTATA... |