HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869032_240869035delinsTAGG , CM000664.2:g.240869032_240869035delinsTAGG | GRCh38 |
NC_000002.11:g.241808449_241808452delinsTAGG , CM000664.1:g.241808449_241808452delinsTAGG | GRCh37 |
NC_000002.10:g.241457122_241457125delinsTAGG | NCBI36 |
NG_008005.1:g.5288_5291delinsTAGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.165+2_165+5delinsTAGG MANE Select | ENSP00000302620.3:n.165+2_165+5delinsTAGG... | |
ENST00000307503.3:c.165+2_165+5delinsTAGG | ENSP00000302620.3:n.165+2_165+5delinsTAGG... | |
ENST00000472436.1:n.185+2_185+5delinsTAGG | ||
NM_000030.2:c.165+2_165+5delinsTAGG | NP_000021.1:n.165+2_165+5delinsTAGG | |
XR_924060.1:n.405+1198_405+1201delinsCCTA | ||
NM_000030.3:c.165+2_165+5delinsTAGG MANE Select | NP_000021.1:n.165+2_165+5delinsTAGG |