HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43928801T>A , CM000684.2:g.43928801T>A | GRCh38 |
NC_000022.10:g.44324681T>A , CM000684.1:g.44324681T>A | GRCh37 |
NC_000022.9:g.42656014T>A | NCBI36 |
NG_008631.1:g.10063T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216180.8:c.421-23T>A MANE Select | ENSP00000216180.3:n.421-23T>A | |
ENST00000216180.7:c.421-23T>A | ENSP00000216180.3:n.421-23T>A | |
ENST00000406117.6:c.*53-23T>A | ENSP00000384668.2:n.*53-23T>A | |
ENST00000423180.2:c.409-23T>A | ENSP00000397987.2:n.409-23T>A | |
ENST00000478713.1:n.455-23T>A | ||
NM_025225.2:c.421-23T>A | NP_079501.2:n.421-23T>A | |
NM_025225.3:c.421-23T>A MANE Select | NP_079501.2:n.421-23T>A |