HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882345T>G , CM000663.2:g.160882345T>G | GRCh38 |
NC_000001.10:g.160852135T>G , CM000663.1:g.160852135T>G | GRCh37 |
NC_000001.9:g.159118759T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.158-141A>C MANE Select | ENSP00000323587.3:n.158-141A>C | |
ENST00000326245.3:c.158-141A>C | ENSP00000323587.3:n.158-141A>C | |
NM_017625.2:c.158-141A>C | NP_060095.2:n.158-141A>C | |
NM_017625.3:c.158-141A>C MANE Select | NP_060095.2:n.158-141A>C |