HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52675230T>A , CM000674.2:g.52675230T>A | GRCh38 |
NC_000012.11:g.53069014T>A , CM000674.1:g.53069014T>A | GRCh37 |
NC_000012.10:g.51355281T>A | NCBI36 |
NG_008364.1:g.10178A>T | |
NG_008364.2:g.10178A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252244.3:c.1898A>T MANE Select | ENSP00000252244.3:p.Lys633Met | |
NM_006121.3:c.1898A>T | NP_006112.3:p.Lys633Met | |
NM_006121.4:c.1898A>T MANE Select | NP_006112.3:p.Lys633Met |