HGVS | Genome Assembly |
---|---|
NC_000022.11:g.46111790T>C , CM000684.2:g.46111790T>C | GRCh38 |
NC_000022.10:g.46507670T>C , CM000684.1:g.46507670T>C | GRCh37 |
NC_000022.9:g.44886334T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_027033.2:n.2579T>C | ||
NR_110479.1:n.2428T>C |