HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149798590T>C , CM000664.2:g.149798590T>C | GRCh38 |
NC_000002.11:g.150655104T>C , CM000664.1:g.150655104T>C | GRCh37 |
NC_000002.10:g.150363350T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_110240.1:n.536-49319T>C (MMADHC-DT) | ||
NR_145421.1:n.1341+5592A>G (LINC01931) |