HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869389_240869390insATCCAGGGCCAT , CM000664.2:g.240869389_240869390insATCCAGGGCCAT | GRCh38 |
NC_000002.11:g.241808806_241808807insATCCAGGGCCAT , CM000664.1:g.241808806_241808807insATCCAGGGCCAT | GRCh37 |
NC_000002.10:g.241457479_241457480insATCCAGGGCCAT | NCBI36 |
NG_008005.1:g.5645_5646insATCCAGGGCCAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.358+27_358+28insATCCAGGGCCAT MANE Select | ENSP00000302620.3:n.358+27_358+28insATCCA... | |
ENST00000307503.3:c.358+27_358+28insATCCAGGGCCAT | ENSP00000302620.3:n.358+27_358+28insATCCA... | |
ENST00000472436.1:n.378+27_378+28insATCCAGGGCCAT | ||
NM_000030.2:c.358+27_358+28insATCCAGGGCCAT | NP_000021.1:n.358+27_358+28insATCCAGGGCCA... | |
XR_924060.1:n.405+843_405+844insATGGCCCTGGAT | ||
NM_000030.3:c.358+27_358+28insATCCAGGGCCAT MANE Select | NP_000021.1:n.358+27_358+28insATCCAGGGCCA... |