HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442613A>T , CM000666.2:g.177442613A>T | GRCh38 |
NC_000004.11:g.178363767A>T , CM000666.1:g.178363767A>T | GRCh37 |
NC_000004.10:g.178600761A>T | NCBI36 |
NG_011845.2:g.4891T>A |
HGVS | Amino-acid Change | |
---|---|---|
XR_001741929.1:n.82+32A>T |