HGVS | Genome Assembly |
---|---|
NC_000004.12:g.77215771C>A , CM000666.2:g.77215771C>A | GRCh38 |
NC_000004.11:g.78136924C>A , CM000666.1:g.78136924C>A | GRCh37 |
NC_000004.10:g.78355948C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000497512.5:n.1675+23504C>A | ||
ENST00000514756.1:n.101+23504C>A |