HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49130929del , CM000665.2:g.49130929del | GRCh38 |
NC_000003.11:g.49168362del , CM000665.1:g.49168362del | GRCh37 |
NC_000003.10:g.49143366del | NCBI36 |
NG_008094.1:g.7240del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.915+23del MANE Select | ENSP00000307156.4:n.915+23del | |
ENST00000305544.8:c.915+23del | ENSP00000307156.4:n.915+23del | |
ENST00000418109.5:c.915+23del | ENSP00000388325.1:n.915+23del | |
NM_002292.3:c.915+23del | NP_002283.3:n.915+23del | |
XM_005265127.3:c.915+23del | XP_005265184.1:n.915+23del | |
XM_005265127.4:c.915+23del | XP_005265184.1:n.915+23del | |
NM_002292.4:c.915+23del MANE Select | NP_002283.3:n.915+23del |