HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044019_114044020insAGACG , CM000672.2:g.114044019_114044020insAGACG | GRCh38 |
NC_000010.10:g.115803778_115803779insAGACG , CM000672.1:g.115803778_115803779insAGACG | GRCh37 |
NC_000010.9:g.115793768_115793769insAGACG | NCBI36 |
NG_012187.1:g.4973_4974insAGACG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.-114_-113insAGACG MANE Select | ENSP00000358301.2:n.-114_-113insAGACG | |
NM_000684.3:c.-114_-113insAGACG MANE Select | NP_000675.1:n.-114_-113insAGACG |