HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43928699A>T , CM000684.2:g.43928699A>T | GRCh38 |
NC_000022.10:g.44324579A>T , CM000684.1:g.44324579A>T | GRCh37 |
NC_000022.9:g.42655912A>T | NCBI36 |
NG_008631.1:g.9961A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216180.8:c.421-125A>T MANE Select | ENSP00000216180.3:n.421-125A>T | |
ENST00000216180.7:c.421-125A>T | ENSP00000216180.3:n.421-125A>T | |
ENST00000406117.6:c.*53-125A>T | ENSP00000384668.2:n.*53-125A>T | |
ENST00000423180.2:c.409-125A>T | ENSP00000397987.2:n.409-125A>T | |
ENST00000478713.1:n.455-125A>T | ||
NM_025225.2:c.421-125A>T | NP_079501.2:n.421-125A>T | |
NM_025225.3:c.421-125A>T MANE Select | NP_079501.2:n.421-125A>T |