HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869049_240869050delinsCG , CM000664.2:g.240869049_240869050delinsCG | GRCh38 |
NC_000002.11:g.241808466_241808467delinsCG , CM000664.1:g.241808466_241808467delinsCG | GRCh37 |
NC_000002.10:g.241457139_241457140delinsCG | NCBI36 |
NG_008005.1:g.5305_5306delinsCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.165+19_165+20delinsCG MANE Select | ENSP00000302620.3:n.165+19_165+20delinsCG... | |
ENST00000307503.3:c.165+19_165+20delinsCG | ENSP00000302620.3:n.165+19_165+20delinsCG... | |
ENST00000472436.1:n.185+19_185+20delinsCG | ||
NM_000030.2:c.165+19_165+20delinsCG | NP_000021.1:n.165+19_165+20delinsCG | |
XR_924060.1:n.405+1183_405+1184delinsCG | ||
NM_000030.3:c.165+19_165+20delinsCG MANE Select | NP_000021.1:n.165+19_165+20delinsCG |