HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442551C>T , CM000666.2:g.177442551C>T | GRCh38 |
NC_000004.11:g.178363705C>T , CM000666.1:g.178363705C>T | GRCh37 |
NC_000004.10:g.178600699C>T | NCBI36 |
NG_011845.2:g.4953G>A |
HGVS | Amino-acid Change | |
---|---|---|
XR_001741929.1:n.52C>T |