HGVS | Genome Assembly |
---|---|
NC_000010.11:g.47353476A>T , CM000672.2:g.47353476A>T | GRCh38 |
NC_000010.10:g.48385886T>A , CM000672.1:g.48385886T>A | GRCh37 |
NC_000010.9:g.48005892T>A | NCBI36 |
NG_029718.1:g.10106A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000584701.2:c.3206A>T MANE Select | ENSP00000463151.1:p.Lys1069Met | |
ENST00000584701.1:c.3206A>T | ENSP00000463151.1:p.Lys1069Met | |
NM_002900.2:c.3206A>T | NP_002891.1:p.Lys1069Met | |
NM_002900.3:c.3206A>T MANE Select | NP_002891.1:p.Lys1069Met |