HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442535C>T , CM000666.2:g.177442535C>T | GRCh38 |
NC_000004.11:g.178363689C>T , CM000666.1:g.178363689C>T | GRCh37 |
NC_000004.10:g.178600683C>T | NCBI36 |
NG_011845.2:g.4969G>A |
HGVS | Amino-acid Change | |
---|---|---|
XR_001741929.1:n.36C>T |