HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60649525C= , CM000676.2:g.60649525C= | GRCh38 |
NC_000014.8:g.61116243C= , CM000676.1:g.61116243C= | GRCh37 |
NC_000014.7:g.60185996C= | NCBI36 |
NG_008231.1:g.4913G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000553535.2:n.248+2410G= | ||
ENST00000554986.2:c.42-2948G= | ENSP00000452700.2:n.42-2948G= | |
ENST00000555955.3:n.1197+2410G= |