HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154903940_154903942del , CM000685.2:g.154903940_154903942del | GRCh38 |
NC_000023.10:g.154132215_154132217del , CM000685.1:g.154132215_154132217del | GRCh37 |
NC_000023.9:g.153785409_153785411del | NCBI36 |
NG_011403.1:g.123785_123787del | |
NG_011403.2:g.123785_123787del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5965_5967del MANE Select | ENSP00000353393.4:p.Glu1989del | |
ENST00000360256.8:c.5965_5967del | ENSP00000353393.4:p.Glu1989del | |
NM_000132.3:c.5965_5967del | NP_000123.1:p.Glu1989del | |
XM_011531126.1:c.5860_5862del | XP_011529428.1:p.Glu1954del | |
NM_000132.4:c.5965_5967del MANE Select | NP_000123.1:p.Glu1989del |