HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60649758A= , CM000676.2:g.60649758A= | GRCh38 |
NC_000014.8:g.61116476A= , CM000676.1:g.61116476A= | GRCh37 |
NC_000014.7:g.60186229A= | NCBI36 |
NG_008231.1:g.4680T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000553535.2:n.248+2177T= | ||
ENST00000554986.2:c.42-3181T= | ENSP00000452700.2:n.42-3181T= | |
ENST00000555955.3:n.1197+2177T= |