HGVS | Genome Assembly |
---|---|
NC_000004.12:g.24799688_24799690del , CM000666.2:g.24799688_24799690del | GRCh38 |
NC_000004.11:g.24801310_24801312del , CM000666.1:g.24801310_24801312del | GRCh37 |
NC_000004.10:g.24410408_24410410del | NCBI36 |
NG_012213.1:g.9226_9228del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382120.4:c.167_169del MANE Select | ENSP00000371554.3:p.Asp56del | |
ENST00000382120.3:c.167_169del | ENSP00000371554.3:p.Asp56del | |
NM_003102.2:c.167_169del | NP_003093.2:p.Asp56del | |
XR_427488.1:n.357_359del | ||
NM_003102.3:c.167_169del | NP_003093.2:p.Asp56del | |
NM_003102.4:c.167_169del MANE Select | NP_003093.2:p.Asp56del |