HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42536274T>A , CM000679.2:g.42536274T>A | GRCh38 |
NC_000017.10:g.40688292T>A , CM000679.1:g.40688292T>A | GRCh37 |
NC_000017.9:g.37941818T>A | NCBI36 |
NG_011552.1:g.5342T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225927.7:c.2T>A MANE Select | ENSP00000225927.1:p.Met1Lys | |
ENST00000225927.6:c.2T>A | ENSP00000225927.1:p.Met1Lys | |
NM_000263.3:c.2T>A | NP_000254.2:p.Met1Lys | |
XM_024450771.1:c.2T>A | XP_024306539.1:p.Met1Lys | |
NM_000263.4:c.2T>A MANE Select | NP_000254.2:p.Met1Lys |