HGVS | Genome Assembly |
---|---|
NC_000004.12:g.102499927C>T , CM000666.2:g.102499927C>T | GRCh38 |
NC_000004.11:g.103421084C>T , CM000666.1:g.103421084C>T | GRCh37 |
NC_000004.10:g.103640116C>T | NCBI36 |
NG_050628.1:g.3599C>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011532467.1:c.643+1322G>A | XP_011530769.1:n.643+1322G>A | |
NR_136202.1:n.48+2512G>A |