HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24258932T= , CM000676.2:g.24258932T= | GRCh38 |
NC_000014.8:g.24728138T= , CM000676.1:g.24728138T= | GRCh37 |
NC_000014.7:g.23797978T= | NCBI36 |
NG_007150.1:g.9235A= | |
NG_007150.2:g.9235A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000206765.11:c.1159+143A= MANE Select | ENSP00000206765.6:n.1159+143A= | |
ENST00000206765.10:c.1159+143A= | ENSP00000206765.6:n.1159+143A= | |
ENST00000544573.5:c.-28-544A= | ENSP00000439446.1:n.-28-544A= | |
ENST00000559136.1:c.232+143A= | ENSP00000453337.1:n.232+143A= | |
NM_000359.2:c.1159+143A= | NP_000350.1:n.1159+143A= | |
NM_000359.3:c.1159+143A= MANE Select | NP_000350.1:n.1159+143A= |