HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869264_240869275del , CM000664.2:g.240869264_240869275del | GRCh38 |
NC_000002.11:g.241808681_241808692del , CM000664.1:g.241808681_241808692del | GRCh37 |
NC_000002.10:g.241457354_241457365del | NCBI36 |
NG_008005.1:g.5520_5531del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.260_271del MANE Select | ENSP00000302620.3:p.Glu87_Leu90del | |
ENST00000307503.3:c.260_271del | ENSP00000302620.3:p.Glu87_Leu90del | |
ENST00000472436.1:n.280_291del | ||
NM_000030.2:c.260_271del | NP_000021.1:p.Glu87_Leu90del | |
XR_924060.1:n.405+965_405+976del | ||
NM_000030.3:c.260_271del MANE Select | NP_000021.1:p.Glu87_Leu90del |