HGVS | Genome Assembly |
---|---|
NC_000004.12:g.144601395A= , CM000666.2:g.144601395A= | GRCh38 |
NC_000004.11:g.145522547A= , CM000666.1:g.145522547A= | GRCh37 |
NC_000004.10:g.145741997A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649263.1:c.328-185417T= | ENSP00000497507.1:n.328-185417T= |