HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877415_240877416del , CM000664.2:g.240877415_240877416del | GRCh38 |
NC_000002.11:g.241816832_241816833del , CM000664.1:g.241816832_241816833del | GRCh37 |
NC_000002.10:g.241465505_241465506del | NCBI36 |
NG_008005.1:g.13671_13672del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.847-122_847-121del MANE Select | ENSP00000302620.3:n.847-122_847-121del | |
ENST00000307503.3:c.847-122_847-121del | ENSP00000302620.3:n.847-122_847-121del | |
ENST00000470255.1:n.503_504del | ||
NM_000030.2:c.847-122_847-121del | NP_000021.1:n.847-122_847-121del | |
NM_000030.3:c.847-122_847-121del MANE Select | NP_000021.1:n.847-122_847-121del |