HGVS | Genome Assembly |
---|---|
NC_000014.9:g.51610427T= , CM000676.2:g.51610427T= | GRCh38 |
NC_000014.8:g.52077145T= , CM000676.1:g.52077145T= | GRCh37 |
NC_000014.7:g.51146895T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000356218.8:c.-147+40017T= | ENSP00000348550.4:n.-147+40017T= | |
ENST00000554745.1:n.278-33025T= | ||
ENST00000556137.5:n.508+40017T= | ||
NM_001042481.2:c.-147+40017T= | NP_001035946.1:n.-147+40017T= | |
XM_011536423.1:c.-147+40017T= | XP_011534725.1:n.-147+40017T= | |
XM_011536424.1:c.-147+40017T= | XP_011534726.1:n.-147+40017T= | |
XM_024449472.1:c.-147+40017T= | XP_024305240.1:n.-147+40017T= | |
XM_024449473.1:c.-146-79264T= | XP_024305241.1:n.-146-79264T= | |
NM_001042481.3:c.-147+40017T= | NP_001035946.1:n.-147+40017T= |