HGVS | Genome Assembly |
---|---|
NC_000006.12:g.22131674T>C , CM000668.2:g.22131674T>C | GRCh38 |
NC_000006.11:g.22131903T>C , CM000668.1:g.22131903T>C | GRCh37 |
NC_000006.10:g.22239882T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_015410.1:n.1391+20754T>C | ||
NR_015410.2:n.1422+20754T>C |