HGVS | Genome Assembly |
---|---|
NC_000013.11:g.107219298T= , CM000675.2:g.107219298T= | GRCh38 |
NC_000013.10:g.107871646T= , CM000675.1:g.107871646T= | GRCh37 |
NC_000013.9:g.106669647T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375915.4:c.916-8543A= MANE Select | ENSP00000365080.1:n.916-8543A= | |
ENST00000375915.3:c.916-8543A= | ENSP00000365080.1:n.916-8543A= | |
NM_001080396.2:c.916-8543A= | NP_001073865.1:n.916-8543A= | |
XM_011521109.1:c.916-8543A= | XP_011519411.1:n.916-8543A= | |
XM_011521109.3:c.916-8543A= | XP_011519411.1:n.916-8543A= | |
NM_001080396.3:c.916-8543A= MANE Select | NP_001073865.1:n.916-8543A= |