HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24278034T= , CM000668.2:g.24278034T= | GRCh38 |
NC_000006.11:g.24278262T= , CM000668.1:g.24278262T= | GRCh37 |
NC_000006.10:g.24386241T= | NCBI36 |
NG_012829.1:g.85019A= | |
NG_012829.2:g.110259A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.922+15A= MANE Select | ENSP00000367715.3:n.922+15A= | |
ENST00000378454.7:c.922+15A= | ENSP00000367715.3:n.922+15A= | |
NM_001195610.1:c.922+15A= | NP_001182539.1:n.922+15A= | |
NM_016356.4:c.922+15A= | NP_057440.2:n.922+15A= | |
NM_016356.5:c.922+15A= MANE Select | NP_057440.2:n.922+15A= | |
NM_001195610.2:c.922+15A= | NP_001182539.1:n.922+15A= |