HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99149749C>T , CM000666.2:g.99149749C>T | GRCh38 |
NC_000004.11:g.100070906C>T , CM000666.1:g.100070906C>T | GRCh37 |
NC_000004.10:g.100289929C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000504581.1:n.170-6969G>A | ||
NR_037884.1:n.680-4796C>T |