HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135894564G>T , CM000667.2:g.135894564G>T | GRCh38 |
NC_000005.9:g.135230253G>T , CM000667.1:g.135230253G>T | GRCh37 |
NC_000005.8:g.135258152G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274520.2:c.184-413C>A MANE Select | ENSP00000274520.1:n.184-413C>A | |
ENST00000274520.1:c.184-413C>A | ENSP00000274520.1:n.184-413C>A | |
NM_000590.1:c.184-413C>A | NP_000581.1:n.184-413C>A | |
NM_000590.2:c.184-413C>A MANE Select | NP_000581.1:n.184-413C>A |