HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107717406T>A , CM000669.2:g.107717406T>A | GRCh38 |
NC_000007.13:g.107357851T>A , CM000669.1:g.107357851T>A | GRCh37 |
NC_000007.12:g.107145087T>A | NCBI36 |
NG_008489.1:g.61772T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.*1960T>A MANE Select | ENSP00000494017.1:n.*1960T>A | |
ENST00000265715.7:c.*1960T>A | ENSP00000265715.3:n.*1960T>A | |
NM_000441.1:c.*1960T>A | NP_000432.1:n.*1960T>A | |
NM_000441.2:c.*1960T>A MANE Select | NP_000432.1:n.*1960T>A |