HGVS | Genome Assembly |
---|---|
NC_000006.12:g.26200449A>T , CM000668.2:g.26200449A>T | GRCh38 |
NC_000006.11:g.26200677A>T , CM000668.1:g.26200677A>T | GRCh37 |
NC_000006.10:g.26308656A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356530.5:c.*510A>T | ENSP00000348924.3:n.*510A>T |