HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114043941_114043942insAGC , CM000672.2:g.114043941_114043942insAGC | GRCh38 |
NC_000010.10:g.115803700_115803701insAGC , CM000672.1:g.115803700_115803701insAGC | GRCh37 |
NC_000010.9:g.115793690_115793691insAGC | NCBI36 |
NG_012187.1:g.4895_4896insAGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.-192_-191insAGC MANE Select | ENSP00000358301.2:n.-192_-191insAGC | |
NM_000684.3:c.-192_-191insAGC MANE Select | NP_000675.1:n.-192_-191insAGC |