HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877591_240877593delinsGCG , CM000664.2:g.240877591_240877593delinsGCG | GRCh38 |
NC_000002.11:g.241817008_241817010delinsGCG , CM000664.1:g.241817008_241817010delinsGCG | GRCh37 |
NC_000002.10:g.241465681_241465683delinsGCG | NCBI36 |
NG_008005.1:g.13847_13849delinsGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.901_903delinsGCG MANE Select | ENSP00000302620.3:p.Arg301Ala | |
ENST00000307503.3:c.901_903delinsGCG | ENSP00000302620.3:p.Arg301Ala | |
ENST00000470255.1:n.679_681delinsGCG | ||
NM_000030.2:c.901_903delinsGCG | NP_000021.1:p.Arg301Ala | |
NM_000030.3:c.901_903delinsGCG MANE Select | NP_000021.1:p.Arg301Ala |