HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445219G>A , CM000673.2:g.2445219G>A | GRCh38 |
NC_000011.9:g.2466449G>A , CM000673.1:g.2466449G>A | GRCh37 |
NC_000011.8:g.2423025G>A | NCBI36 |
NG_008935.1:g.5229G>A , LRG_287:g.5229G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.24-164G>A | ENSP00000434560.2:n.24-164G>A | |
ENST00000646564.2:c.121G>A | ENSP00000495806.2:p.Ala41Thr | |
ENST00000155840.12:c.121G>A MANE Select | ENSP00000155840.2:p.Ala41Thr | |
ENST00000155840.9:c.121G>A | ENSP00000155840.2:p.Ala41Thr | |
ENST00000496887.6:c.24-164G>A | ENSP00000434560.1:n.24-164G>A | |
NM_000218.2:c.121G>A , LRG_287t1:c.121G>A | NP_000209.2:p.Ala41Thr | |
NM_000218.3:c.121G>A MANE Select | NP_000209.2:p.Ala41Thr |