HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114705893_114705894insG , CM000663.2:g.114705893_114705894insG | GRCh38 |
NC_000001.10:g.115248514_115248515insG , CM000663.1:g.115248514_115248515insG | GRCh37 |
NC_000001.9:g.115050037_115050038insG | NCBI36 |
NG_007572.1:g.16001_16002insC , LRG_92:g.16001_16002insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.*2200_*2201insC MANE Select | ENSP00000358548.4:n.*2200_*2201insC | |
ENST00000369535.4:c.*2200_*2201insC | ENSP00000358548.4:n.*2200_*2201insC | |
NM_002524.4:c.*2200_*2201insC | NP_002515.1:n.*2200_*2201insC | |
NM_002524.5:c.*2200_*2201insC MANE Select | NP_002515.1:n.*2200_*2201insC |