HGVS | Genome Assembly |
---|---|
NC_000002.12:g.233618450_233618451delinsCA , CM000664.2:g.233618450_233618451delinsCA | GRCh38 |
NC_000002.11:g.234527096_234527097delinsCA , CM000664.1:g.234527096_234527097delinsCA | GRCh37 |
NC_000002.10:g.234191835_234191836delinsCA | NCBI36 |
NG_002601.2:g.33707_33708delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373450.5:c.743_744delinsCA MANE Select | ENSP00000362549.4:p.Thr248= | |
ENST00000373450.4:c.743_744delinsCA | ENSP00000362549.4:p.Thr248= | |
NM_019076.4:c.743_744delinsCA | NP_061949.3:p.Thr248= | |
NM_019076.5:c.743_744delinsCA MANE Select | NP_061949.3:p.Thr248= |