HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443335dup , CM000668.2:g.32443335dup | GRCh38 |
NC_000006.11:g.32411112dup , CM000668.1:g.32411112dup | GRCh37 |
NC_000006.10:g.32519090dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.479dup MANE Select | ENSP00000378786.2:p.Val161SerfsTer23 | |
ENST00000374982.5:c.404dup | ENSP00000364121.5:p.Val136SerfsTer23 | |
ENST00000395388.6:c.479dup | ENSP00000378786.2:p.Val161SerfsTer23 | |
NM_019111.4:c.479dup | NP_061984.2:p.Val161SerfsTer23 | |
NM_019111.5:c.479dup MANE Select | NP_061984.2:p.Val161SerfsTer23 |