HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114044022T>A , CM000672.2:g.114044022T>A | GRCh38 |
NC_000010.10:g.115803781T>A , CM000672.1:g.115803781T>A | GRCh37 |
NC_000010.9:g.115793771T>A | NCBI36 |
NG_012187.1:g.4976T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.-111T>A MANE Select | ENSP00000358301.2:n.-111T>A | |
NM_000684.3:c.-111T>A MANE Select | NP_000675.1:n.-111T>A |