HGVS | Genome Assembly |
---|---|
NC_000004.12:g.6269372C>T , CM000666.2:g.6269372C>T | GRCh38 |
NC_000004.11:g.6271099C>T , CM000666.1:g.6271099C>T | GRCh37 |
NC_000004.10:g.6322000C>T | NCBI36 |
NG_011700.1:g.4523C>T |
HGVS | Amino-acid change | |
---|---|---|
XM_017008586.1:c.4+7733C>T | XP_016864075.1:n.4+7733C>T |