HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111673del , CM000670.2:g.118111673del | GRCh38 |
NC_000008.10:g.119123912del , CM000670.1:g.119123912del | GRCh37 |
NC_000008.9:g.119193093del | NCBI36 |
NG_007455.2:g.5151del , LRG_493:g.5151del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-623del MANE Select | ENSP00000367446.3:n.-623del | |
ENST00000378204.6:c.-623del | ENSP00000367446.2:n.-623del | |
NM_000127.2:c.-623del , LRG_493t1:c.-623del | NP_000118.2:n.-623del | |
NM_000127.3:c.-623del MANE Select | NP_000118.2:n.-623del |