HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99149626A>C , CM000666.2:g.99149626A>C | GRCh38 |
NC_000004.11:g.100070783A>C , CM000666.1:g.100070783A>C | GRCh37 |
NC_000004.10:g.100289806A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000504581.1:n.170-6846T>G | ||
NR_037884.1:n.680-4919A>C |