HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63511904T= , CM000679.2:g.63511904T= | GRCh38 |
NC_000017.10:g.61589265T= , CM000679.1:g.61589265T= | GRCh37 |
NC_000017.9:g.58942997T= | NCBI36 |
HGVS | Amino-acid Change |
---|---|
ENST00000423435.2:n.1288+1072T= | |
ENST00000577647.2:c.*1343+1072T= | ENSP00000464149.1:n.*1343+1072T= |