HGVS | Genome Assembly |
---|---|
NC_000012.12:g.105714823T>C , CM000674.2:g.105714823T>C | GRCh38 |
NC_000012.11:g.106108601T>C , CM000674.1:g.106108601T>C | GRCh37 |
NC_000012.10:g.104632731T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_110108.1:n.54+10567T>C | ||
NR_110109.1:n.55-339T>C | ||
NR_110110.1:n.83+7967T>C | ||
NR_110111.1:n.83+7967T>C | ||
NR_110111.2:n.83+7967T>C |