HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161802T>A , CM000668.2:g.28161802T>A | GRCh38 |
NC_000006.11:g.28129580T>A , CM000668.1:g.28129580T>A | GRCh37 |
NC_000006.10:g.28237559T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.34T>A | ||
ENST00000440790.6:n.22T>A | ||
ENST00000570126.1:n.11T>A | ||
NR_103448.1:n.42T>A |