HGVS | Genome Assembly |
---|---|
NC_000011.10:g.36350117A= , CM000673.2:g.36350117A= | GRCh38 |
NC_000011.9:g.36371667A= , CM000673.1:g.36371667A= | GRCh37 |
NC_000011.8:g.36328243A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000530639.6:c.-125-50880A= MANE Select | ENSP00000435050.1:n.-125-50880A= | |
ENST00000527172.5:c.-291-43729A= | ENSP00000433708.1:n.-291-43729A= | |
ENST00000529034.5:n.152-50880A= | ||
ENST00000530639.5:c.-125-50880A= | ENSP00000435050.1:n.-125-50880A= | |
ENST00000532121.5:c.-126+52A= | ENSP00000433893.1:n.-126+52A= | |
NM_001160167.1:c.-125-50880A= | NP_001153639.1:n.-125-50880A= | |
NM_001160167.2:c.-125-50880A= MANE Select | NP_001153639.1:n.-125-50880A= |