HGVS | Genome Assembly |
---|---|
NC_000021.9:g.35161365C>T , CM000683.2:g.35161365C>T | GRCh38 |
NC_000021.8:g.36533662C>T , CM000683.1:g.36533662C>T | GRCh37 |
NC_000021.7:g.35455532C>T | NCBI36 |
NG_011402.2:g.828347G>A , LRG_482:g.828347G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000475045.6:c.-196-96293G>A | ENSP00000477072.1:n.-196-96293G>A |