HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882256_160882257insG , CM000663.2:g.160882256_160882257insG | GRCh38 |
NC_000001.10:g.160852046_160852047insG , CM000663.1:g.160852046_160852047insG | GRCh37 |
NC_000001.9:g.159118670_159118671insG | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000326245.4:c.158-53_158-52insC MANE Select | ENSP00000323587.3:n.158-53_158-52insC | |
ENST00000326245.3:c.158-53_158-52insC | ENSP00000323587.3:n.158-53_158-52insC | |
ENST00000464077.1:n.39_40insC | ||
NM_017625.2:c.158-53_158-52insC | NP_060095.2:n.158-53_158-52insC | |
NM_017625.3:c.158-53_158-52insC MANE Select | NP_060095.2:n.158-53_158-52insC |