HGVS | Genome Assembly |
---|---|
NC_000006.12:g.55283206C>T , CM000668.2:g.55283206C>T | GRCh38 |
NC_000006.11:g.55148004C>T , CM000668.1:g.55148004C>T | GRCh37 |
NC_000006.10:g.55255963C>T | NCBI36 |
NG_012447.1:g.113934C>T | |
NG_012447.2:g.181747C>T |
HGVS | Amino-acid change | |
---|---|---|
XM_017010798.1:c.1331+756C>T | XP_016866287.1:n.1331+756C>T |