HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46010966G>A , CM000682.2:g.46010966G>A | GRCh38 |
NC_000020.10:g.44639605G>A , CM000682.1:g.44639605G>A | GRCh37 |
NC_000020.9:g.44073012G>A | NCBI36 |
NG_011468.1:g.7059G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.565G>A MANE Select | ENSP00000361405.3:p.Ala189Thr | |
NM_004994.2:c.565G>A | NP_004985.2:p.Ala189Thr | |
NM_004994.3:c.565G>A MANE Select | NP_004985.2:p.Ala189Thr |