HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19966820T>A , CM000670.2:g.19966820T>A | GRCh38 |
NC_000008.10:g.19824331T>A , CM000670.1:g.19824331T>A | GRCh37 |
NC_000008.9:g.19868611T>A | NCBI36 |
NG_008855.1:g.32750T>A | |
NG_008855.2:g.70104T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.*1510T>A MANE Select | ENSP00000497642.1:n.*1510T>A | |
ENST00000650478.1:c.1878T>A | ENSP00000497560.1:n.1878T>A | |
ENST00000311322.8:c.*1510T>A | ENSP00000309757.6:n.*1510T>A | |
NM_000237.2:c.*1510T>A | NP_000228.1:n.*1510T>A | |
NM_000237.3:c.*1510T>A MANE Select | NP_000228.1:n.*1510T>A |