HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304455_152304456delinsAC , CM000663.2:g.152304455_152304456delinsAC | GRCh38 |
NC_000001.10:g.152276931_152276932delinsAC , CM000663.1:g.152276931_152276932delinsAC | GRCh37 |
NC_000001.9:g.150543555_150543556delinsAC | NCBI36 |
NG_016190.1:g.25748_25749delinsGT , LRG_1028:g.25748_25749delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.10430_10431delinsGT MANE Select | ENSP00000357789.1:p.Arg3477= | |
ENST00000368799.1:c.10430_10431delinsGT | ENSP00000357789.1:p.Arg3477= | |
NM_002016.1:c.10430_10431delinsGT , LRG_1028t1:c.10430_10431delinsGT | NP_002007.1:p.Arg3477= | |
XM_011509329.1:c.9109-623_9109-622delinsGT | XP_011507631.1:n.9109-623_9109-622delinsGT | |
NM_002016.2:c.10430_10431delinsGT MANE Select | NP_002007.1:p.Arg3477= |