HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204190415_204190416insG , CM000663.2:g.204190415_204190416insG | GRCh38 |
NC_000001.10:g.204159543_204159544insG , CM000663.1:g.204159543_204159544insG | GRCh37 |
NC_000001.9:g.202426166_202426167insG | NCBI36 |
NG_032151.1:g.11076_11077insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367194.5:c.*68_*69insC MANE Select | ENSP00000356162.4:n.*68_*69insC | |
ENST00000367194.4:c.*68_*69insC | ENSP00000356162.4:n.*68_*69insC | |
NM_002256.3:c.*68_*69insC | NP_002247.3:n.*68_*69insC | |
XM_011509525.1:c.*68_*69insC | XP_011507827.1:n.*68_*69insC | |
NM_002256.4:c.*68_*69insC MANE Select | NP_002247.3:n.*68_*69insC |