HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152648415_152648416insG , CM000669.2:g.152648415_152648416insG | GRCh38 |
NC_000007.13:g.152345500_152345501insG , CM000669.1:g.152345500_152345501insG | GRCh37 |
NC_000007.12:g.151976433_151976434insG | NCBI36 |
NG_027988.1:g.32750_32751insC | |
NG_027988.2:g.32750_32751insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698506.1:c.*226_*227insC | ENSP00000513758.1:n.*226_*227insC | |
ENST00000359321.2:c.*226_*227insC MANE Select | ENSP00000352271.1:n.*226_*227insC | |
ENST00000359321.1:c.*226_*227insC | ENSP00000352271.1:n.*226_*227insC | |
ENST00000495707.1:n.1091_1092insC | ||
NM_005431.1:c.*226_*227insC | NP_005422.1:n.*226_*227insC | |
NM_005431.2:c.*226_*227insC MANE Select | NP_005422.1:n.*226_*227insC |